Clinical, biochemical and molecular characterization of a new case with FDX2‐related mitochondrial disorder: Potential biomarkers and treatment options.

Autor: Wongkittichote, Parith, Pantano, Cassandra, He, Miao, Hong, Xinying, Demczko, Matthew M.

Publikováno v: Journal of Inherited Metabolic Disease Reports; Mar2024, Vol. 65 Issue 2, p102-109, 8p

Clinical, biochemical and molecular characterization of a new case with FDX2 -related mitochondrial disorder: Potential biomarkers and treatment options.

Autor: Wongkittichote P; Division of Human Genetics Children's Hospital of Philadelphia Philadelphia Pennsylvania USA.; Department of Pathology and Laboratory Medicine Children's Hospital of Philadelphia Philadelphia Pennsylvania USA.; Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital Mahidol University Bangkok Thailand., Pantano C; Division of Human Genetics Children's Hospital of Philadelphia Philadelphia Pennsylvania USA., He M; Department of Pathology and Laboratory Medicine Children's Hospital of Philadelphia Philadelphia Pennsylvania USA.; University of Pennsylvania, Perelman School of Medicine Philadelphia Pennsylvania USA., Hong X; Department of Pathology and Laboratory Medicine Children's Hospital of Philadelphia Philadelphia Pennsylvania USA.; University of Pennsylvania, Perelman School of Medicine Philadelphia Pennsylvania USA., Demczko MM; Division of Human Genetics Children's Hospital of Philadelphia Philadelphia Pennsylvania USA.; University of Pennsylvania, Perelman School of Medicine Philadelphia Pennsylvania USA.

Publikováno v: JIMD reports [JIMD Rep] 2024 Jan 23; Vol. 65 (2), pp. 102-109. Date of Electronic Publication: 2024 Jan 23 (Print Publication: 2024).