One potential hotspot SLC25A20 gene variants in Chinese patients with carnitine-acylcarnitine translocase deficiency

BACKGROUND: Carnitine-acylcarnitine translocase deficiency (CACT deficiency) is a rare and life-threatening autosomal recessive disorder of mitochondrial fatty acid oxidation caused by variant of SLC25A20 gene. The most prevalent missense variant in the SLC25A20 gene in Asia was c.199–10T > G. Du...

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Detalles Bibliográficos
Autores principales: Li, Xiaoli, Shen, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676358/
https://www.ncbi.nlm.nih.gov/pubmed/36419912
http://dx.doi.org/10.3389/fped.2022.1029004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676358/
https://www.ncbi.nlm.nih.gov/pubmed/36419912
http://dx.doi.org/10.3389/fped.2022.1029004

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