The discovery of AGK's historical breakthrough. | Download Scientific Diagram
What is AGK Gene Sengers syndrome NGS Genetic DNA Test ?
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
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
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
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
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
INBORN ERRORS OF METABOLISM
Discovery-driven research leads to breakthrough in understanding rare Sengers syndrome
AGK regulates the progression to NASH by affecting mitochondria complex I function
Sengers syndrome (Concept Id: C1859317)
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria - ScienceDirect
Noonan syndrome - The Lancet
Sengers Syndrome | Hereditary Ocular Diseases
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
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
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
