Leukodystrophy Associated with Mitochondrial Complex 1 Deficiency Due to Mutation in NUBPL Gene—An Unusual Follow-Up Finding

Detalles Bibliográficos
Autores principales: Peter S, Babu, Vandana G, Sree
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Medical and Scientific Publishers Pvt. Ltd. 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968539/
https://www.ncbi.nlm.nih.gov/pubmed/36855717
http://dx.doi.org/10.1055/s-0042-1758195

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968539/
https://www.ncbi.nlm.nih.gov/pubmed/36855717
http://dx.doi.org/10.1055/s-0042-1758195

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