![Sengers syndrome in Asian Indians – two novel mutations and variant phenotype-genotype correlation - IOS Press Sengers syndrome in Asian Indians – two novel mutations and variant phenotype-genotype correlation - IOS Press](https://content.iospress.com/media/trd/2017/2-3-4/trd-2-3-4-trd017/trd-2-trd017-g001.jpg?width=755)
Sengers syndrome in Asian Indians – two novel mutations and variant phenotype-genotype correlation - IOS Press
![Mitochondrial disease in children - Rahman - 2020 - Journal of Internal Medicine - Wiley Online Library Mitochondrial disease in children - Rahman - 2020 - Journal of Internal Medicine - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/b23e9762-5387-4155-8205-d72e00ddc3fe/joim13054-toc-0001-m.jpg)
Mitochondrial disease in children - Rahman - 2020 - Journal of Internal Medicine - Wiley Online Library
![IJMS | Free Full-Text | Characterization of a Novel Splicing Variant in Acylglycerol Kinase (AGK) Associated with Fatal Sengers Syndrome IJMS | Free Full-Text | Characterization of a Novel Splicing Variant in Acylglycerol Kinase (AGK) Associated with Fatal Sengers Syndrome](https://www.mdpi.com/ijms/ijms-22-13484/article_deploy/html/images/ijms-22-13484-g002-550.jpg)
IJMS | Free Full-Text | Characterization of a Novel Splicing Variant in Acylglycerol Kinase (AGK) Associated with Fatal Sengers Syndrome
![Media Release: Discovery-driven research leads to breakthrough in understanding rare Sengers syndrome | Bio21 Molecular Science & Biotechnology Institute Media Release: Discovery-driven research leads to breakthrough in understanding rare Sengers syndrome | Bio21 Molecular Science & Biotechnology Institute](https://www.bio21.unimelb.edu.au/sites/www.bio21.unimelb.edu.au/files/styles/page/public/field/image/2017-07-17-Bio21-News_Diana-Stojanovski.jpg?itok=IOP6sx5M)
Media Release: Discovery-driven research leads to breakthrough in understanding rare Sengers syndrome | Bio21 Molecular Science & Biotechnology Institute
![Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndrome. - Abstract - Europe PMC Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndrome. - Abstract - Europe PMC](https://europepmc.org/articles/PMC3276657/bin/gr1.jpg)
Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndrome. - Abstract - Europe PMC
Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patie
![Acylglycerol kinase: mitochondrial protein transport meets lipid biosynthesis | 2017 | Publications Archive | Publications | From analysis to synthesis - spanning all domains of life Acylglycerol kinase: mitochondrial protein transport meets lipid biosynthesis | 2017 | Publications Archive | Publications | From analysis to synthesis - spanning all domains of life](https://www.bioss.uni-freiburg.de/fileadmin/user_upload/Images/Pictures_POGO_2017/large/Becker_TCB_2017_l.jpg)
Acylglycerol kinase: mitochondrial protein transport meets lipid biosynthesis | 2017 | Publications Archive | Publications | From analysis to synthesis - spanning all domains of life
Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patie
![Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria - ScienceDirect Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1097276517304409-fx1.jpg)
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria - ScienceDirect
![Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria. | Semantic Scholar Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/ab1142f01c5c41a019cc50a36370e7b610e39cc3/9-Figure5-1.png)
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria. | Semantic Scholar
![Cardiomyopathy, Familial Hypertrophic, 17 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials Cardiomyopathy, Familial Hypertrophic, 17 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials](http://malacards.blob.core.windows.net/network-images-v5-12-8/cardiomyopathy_familial_hypertrophic_17_2_related_diseases.jpg)
Cardiomyopathy, Familial Hypertrophic, 17 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
![Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria. | Semantic Scholar Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/ab1142f01c5c41a019cc50a36370e7b610e39cc3/8-Figure4-1.png)
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria. | Semantic Scholar
Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patie
![Extending the phenotypic spectrum of Sengers syndrome: Congenital lactic acidosis with synthetic liver dysfunction - IOS Press Extending the phenotypic spectrum of Sengers syndrome: Congenital lactic acidosis with synthetic liver dysfunction - IOS Press](https://content.iospress.com/media/trd/2018/3-1/trd-3-1-trd020/trd-3-trd020-g001.jpg?width=755)
Extending the phenotypic spectrum of Sengers syndrome: Congenital lactic acidosis with synthetic liver dysfunction - IOS Press
![Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients | Orphanet Journal of Rare Diseases | Full Text Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients | Orphanet Journal of Rare Diseases | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13023-014-0119-3/MediaObjects/13023_2014_Article_119_Fig2_HTML.jpg)
Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients | Orphanet Journal of Rare Diseases | Full Text
![Genes | Free Full-Text | Molecular Insights into Mitochondrial Protein Translocation and Human Disease Genes | Free Full-Text | Molecular Insights into Mitochondrial Protein Translocation and Human Disease](https://www.mdpi.com/genes/genes-12-01031/article_deploy/html/images/genes-12-01031-g001.png)