Detecting mitochondrial electron transport chain enzyme defects in low-heteroplasmy single large-scale mtDNA deletion syndromes (SLSMDSs).

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Bibliographic Details
Title: Detecting mitochondrial electron transport chain enzyme defects in low-heteroplasmy single large-scale mtDNA deletion syndromes (SLSMDSs).
Authors: Pan X; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, USA., Wang Y; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, USA; Baylor Genetics, Houston, USA., Liu N; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, USA; Baylor Genetics, Houston, USA., Luo X; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, USA; Baylor Genetics, Houston, USA., Sutton VR; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, USA; Baylor Genetics, Houston, USA; Texas Children's Hospital, Houston, USA., Craigen WJ; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, USA; Texas Children's Hospital, Houston, USA., Sun Q; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, USA; Baylor Genetics, Houston, USA. Electronic address: qsun@bcm.edu.
Source: Molecular genetics and metabolism [Mol Genet Metab] 2025 Nov; Vol. 146 (3), pp. 109260. Date of Electronic Publication: 2025 Oct 08.
Publication Type: Journal Article
Journal Info: Publisher: Academic Press Country of Publication: United States NLM ID: 9805456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-7206 (Electronic) Linking ISSN: 10967192 NLM ISO Abbreviation: Mol Genet Metab Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1096-7206
DOI:10.1016/j.ymgme.2025.109260