What is AGK Gene Sengers syndrome NGS Genetic DNA Test ?
Mitochondrial citrate synthase crystals: Novel finding in Sengers syndrome caused by acylglycerol kinase (AGK) mutations - ScienceDirect
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria. | Semantic Scholar
Frontiers | Acylglycerol Kinase-Targeted Therapies in Oncology
Sengers Syndrome-Associated Mitochondrial Acylglycerol Kinase Is a Subunit of the Human TIM22 Protein Import Complex - ScienceDirect
INBORN ERRORS OF METABOLISM
Sengers syndrome in Asian Indians – two novel mutations and variant phenotype-genotype correlation - IOS Press
Mitochondrial diseases | Nature Reviews Disease Primers
Sengers Syndrome: A Rare Cause of HOCM
Cardiomyopathy, Familial Hypertrophic, 17 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
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 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
Discovery-driven research leads to breakthrough in understanding rare Sengers syndrome
Genes | Free Full-Text | Molecular Insights into Mitochondrial Protein Translocation and Human Disease
IJMS | Free Full-Text | Characterization of a Novel Splicing Variant in Acylglycerol Kinase (AGK) Associated with Fatal Sengers Syndrome
Lack of the Mitochondrial Protein Acylglycerol Kinase Causes Sengers Syndrome
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria
Mitochondrial disease in children - Rahman - 2020 - Journal of Internal Medicine - Wiley Online Library
