Cytochrome c oxidase deficiency caused by biallelic SCO2 mutations in two sibs with cerebellar ataxia and progressive peripheral axonal neuropathy

Detalles Bibliográficos
Autores principales: Barcia, Giulia, Assouline, Zahra, Pennisi, Alessandra, Gitiaux, Cyril, Schiff, Manuel, Boddaert, Nathalie, Munnich, Arnold, Bonnefont, Jean-Paul, Rötig, Agnès
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895674/
https://www.ncbi.nlm.nih.gov/pubmed/31844624
http://dx.doi.org/10.1016/j.ymgmr.2019.100528

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895674/
https://www.ncbi.nlm.nih.gov/pubmed/31844624
http://dx.doi.org/10.1016/j.ymgmr.2019.100528

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