Complex I deficiency and Leigh syndrome through the eyes of a clinician

K. Õunap and K. Reinson discuss the biochemical and functional characterization of the NDUFC2 pathogenic variants identified in children with Leigh syndrome by R. Taylor and colleagues, in this issue of EMBO Molecular Medicine [Image: see text]

Detalles Bibliográficos
Autores principales: Reinson, Karit, Õunap, Katrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
News & Views
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645367/
https://www.ncbi.nlm.nih.gov/pubmed/33124751
http://dx.doi.org/10.15252/emmm.202013187
Descripción
Sumario:K. Õunap and K. Reinson discuss the biochemical and functional characterization of the NDUFC2 pathogenic variants identified in children with Leigh syndrome by R. Taylor and colleagues, in this issue of EMBO Molecular Medicine [Image: see text]

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