Correspondence to: “Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency” and “A novel NDUFA1 mutation leads to progressive mitochondrial complex I- specific neurodegenerative disease”

Detalles Bibliográficos
Autores principales: Xu, Jack Junchi, Østergaard, Elsebet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537428/
https://www.ncbi.nlm.nih.gov/pubmed/28794991
http://dx.doi.org/10.1016/j.ymgmr.2017.07.008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5537428/
https://www.ncbi.nlm.nih.gov/pubmed/28794991
http://dx.doi.org/10.1016/j.ymgmr.2017.07.008

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