Lack of the Mitochondrial Protein Acylglycerol Kinase Causes Sengers Syndrome
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
Acylglycerol kinase: mitochondrial protein transport meets lipid biosynthesis | 2017 | Publications Archive | Publications | From analysis to synthesis - spanning all domains of life
AGK regulates the progression to NASH by affecting mitochondria complex I function
Mitochondrial citrate synthase crystals: Novel finding in Sengers syndrome caused by acylglycerol kinase (AGK) mutations - ScienceDirect
Atypical Presentation of Sengers Syndrome: A Novel Mutation Revealed with Postmortem Genetic Testing: Fetal and Pediatric Pathology: Vol 39, No 2
Sengers Syndrome: A Rare Cause of HOCM
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
Figure 1 | Journal of Medical Genetics
Sengers Syndrome-Associated Mitochondrial Acylglycerol Kinase Is a Subunit of the Human TIM22 Protein Import Complex - ScienceDirect
Sengers syndrome (Concept Id: C1859317)
Sengers Syndrome | Hereditary Ocular Diseases
Media Release: Discovery-driven research leads to breakthrough in understanding rare Sengers syndrome | Bio21 Molecular Science & Biotechnology Institute
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
Iowa Donor Network - “After 19 years of fighting heart problems linked to Sengers Syndrome, Chloe needed a life-saving operation in the early hours of Christmas morning. After surviving on ECMO life
Sennetsu Fever disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Sengers Syndrome: A Rare Cause of HOCM
Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patie
Sengers syndrome in Asian Indians – two novel mutations and variant phenotype-genotype correlation - IOS Press
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria - ScienceDirect
Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patie
Frontiers | Acylglycerol Kinase-Targeted Therapies in Oncology
