Sennetsu Fever disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Mitochondrial disease in children - Rahman - 2020 - Journal of Internal Medicine - Wiley Online Library
Two Novel Mutations in the AGK Gene: Two Case Reports with Sengers Syndrome
AGK regulates the progression to NASH by affecting mitochondria complex I function
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. | Semantic Scholar
Sengers Syndrome | Hereditary Ocular Diseases
Sengers Syndrome-Associated Mitochondrial Acylglycerol Kinase Is a Subunit of the Human TIM22 Protein Import Complex - ScienceDirect
Frontiers | Acylglycerol Kinase-Targeted Therapies in Oncology
Cardiomyopathy, Familial Hypertrophic, 17 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
INBORN ERRORS OF METABOLISM
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
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria. | Semantic Scholar
Sengers syndrome in Asian Indians – two novel mutations and variant phenotype-genotype correlation - IOS Press
Extending the phenotypic spectrum of Sengers syndrome: Congenital lactic acidosis with synthetic liver dysfunction - IOS Press
Mitochondrial citrate synthase crystals: Novel finding in Sengers syndrome caused by acylglycerol kinase (AGK) mutations - ScienceDirect
Figure 1 | Journal of Medical Genetics
What is AGK Gene Sengers syndrome NGS Genetic DNA Test ?
Atypical Presentation of Sengers Syndrome: A Novel Mutation Revealed with Postmortem Genetic Testing: Fetal and Pediatric Pathology: Vol 39, No 2
Lack of the Mitochondrial Protein Acylglycerol Kinase Causes Sengers Syndrome
Noonan syndrome - The Lancet
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
Discovery-driven research leads to breakthrough in understanding rare Sengers syndrome
