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Response to the paper titled “Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy”

Detalles Bibliográficos
Autor principal: Graves, Tracey D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6141117/
https://www.ncbi.nlm.nih.gov/pubmed/30254444
http://dx.doi.org/10.2147/NDT.S179068