Sengers syndrome in Asian Indians – two novel mutations and variant phenotype-genotype correlation - IOS Press
Frontiers | Case Report: Two Chinese Infants of Sengers Syndrome Caused by Mutations in AGK Gene
Media Release: Discovery-driven research leads to breakthrough in understanding rare Sengers syndrome | Bio21 Molecular Science & Biotechnology Institute
Mitochondrial disease in children - Rahman - 2020 - Journal of Internal Medicine - Wiley Online Library
Atypical Presentation of Sengers Syndrome: A Novel Mutation Revealed with Postmortem Genetic Testing: Fetal and Pediatric Pathology: Vol 39, No 2
AGK regulates the progression to NASH by affecting mitochondria complex I function
Cardiomyopathy, Familial Hypertrophic, 17 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Sengers Syndrome: A Rare Cause of HOCM
Sennetsu Fever disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Sengers Syndrome | Hereditary Ocular Diseases
Acylglycerol kinase: mitochondrial protein transport meets lipid biosynthesis | 2017 | Publications Archive | Publications | From analysis to synthesis - spanning all domains of life
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 patients | Orphanet Journal of Rare Diseases | Full Text
Lack of the Mitochondrial Protein Acylglycerol Kinase Causes Sengers Syndrome
Genes | Free Full-Text | Molecular Insights into Mitochondrial Protein Translocation and Human Disease
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria - ScienceDirect
INBORN ERRORS OF METABOLISM
Extending the phenotypic spectrum of Sengers syndrome: Congenital lactic acidosis with synthetic liver dysfunction - IOS Press
Figure 1 | Journal of Medical Genetics
Mitochondrial citrate synthase crystals: Novel finding in Sengers syndrome caused by acylglycerol kinase (AGK) mutations - ScienceDirect
Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patie
Sengers Syndrome: A Rare Cause of HOCM
What is AGK Gene Sengers syndrome NGS Genetic DNA Test ?
Sengers Syndrome-Associated Mitochondrial Acylglycerol Kinase Is a Subunit of the Human TIM22 Protein Import Complex - ScienceDirect
