What is AGK Gene Sengers syndrome NGS Genetic DNA Test ?
Discovery-driven research leads to breakthrough in understanding rare 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: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patie
AGK regulates the progression to NASH by affecting mitochondria complex I function
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria
Sengers Syndrome-Associated Mitochondrial Acylglycerol Kinase Is a Subunit of the Human TIM22 Protein Import Complex - ScienceDirect
IJMS | Free Full-Text | Characterization of a Novel Splicing Variant in Acylglycerol Kinase (AGK) Associated with Fatal 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
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
Mitochondrial diseases | Nature Reviews Disease Primers
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria. | Semantic Scholar
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
Sengers syndrome (Concept Id: C1859317)
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria. | Semantic Scholar
Frontiers | Case Report: Two Chinese Infants of Sengers Syndrome Caused by Mutations in AGK Gene
Media Release: Discovery-driven research leads to breakthrough in understanding rare Sengers syndrome | Bio21 Molecular Science & Biotechnology Institute
Sengers Syndrome: A Rare Cause of HOCM
Sengers Syndrome: A Rare Cause of HOCM
Extending the phenotypic spectrum of Sengers syndrome: Congenital lactic acidosis with synthetic liver dysfunction - IOS Press
Mitochondrial disease in children - Rahman - 2020 - Journal of Internal Medicine - Wiley Online Library
Acylglycerol kinase: mitochondrial protein transport meets lipid biosynthesis | 2017 | Publications Archive | Publications | From analysis to synthesis - spanning all domains of life
