Frontiers | Case Report: Two Chinese Infants of Sengers Syndrome Caused by Mutations in AGK Gene
Sengers Syndrome-Associated Mitochondrial Acylglycerol Kinase Is a Subunit of the Human TIM22 Protein Import Complex - ScienceDirect
What is AGK Gene Sengers syndrome NGS Genetic DNA Test ?
Sengers Syndrome: A Rare Cause of HOCM
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 patie
Sengers syndrome in Asian Indians – two novel mutations and variant phenotype-genotype correlation - IOS Press
IJMS | Free Full-Text | Characterization of a Novel Splicing Variant in Acylglycerol Kinase (AGK) Associated with Fatal 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
Sengers syndrome (Concept Id: C1859317)
Two Novel Mutations in the AGK Gene: Two Case Reports with Sengers Syndrome
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
Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patie
Cardiomyopathy, Familial Hypertrophic, 17 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Atypical Presentation of Sengers Syndrome: A Novel Mutation Revealed with Postmortem Genetic Testing: Fetal and Pediatric Pathology: Vol 39, No 2
Mitochondrial disease in children - Rahman - 2020 - Journal of Internal Medicine - Wiley Online Library
Discovery-driven research leads to breakthrough in understanding rare Sengers syndrome
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
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
Mitochondrial disease in children - Rahman - 2020 - Journal of Internal Medicine - Wiley Online Library
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
Media Release: Discovery-driven research leads to breakthrough in understanding rare Sengers syndrome | Bio21 Molecular Science & Biotechnology Institute
Genes | Free Full-Text | Molecular Insights into Mitochondrial Protein Translocation and Human Disease
Mitochondrial diseases | Nature Reviews Disease Primers
Sengers Syndrome | Hereditary Ocular Diseases
INBORN ERRORS OF METABOLISM
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria. | Semantic Scholar
Sennetsu Fever disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria - ScienceDirect
