Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families

Detalles Bibliográficos
Autores principales: Kocoglu, Cemile, Gundogdu, Asli, Kocaman, Gulsen, Kahraman-Koytak, Pinar, Uluc, Kayihan, Kiziltan, Gunes, Caglayan, Ahmet Okay, Bilguvar, Kaya, Vural, Atay, Basak, A. Nazli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2018
Materias:
Clinical/Scientific Notes
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5773845/
https://www.ncbi.nlm.nih.gov/pubmed/29379883
http://dx.doi.org/10.1212/NXG.0000000000000218

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5773845/
https://www.ncbi.nlm.nih.gov/pubmed/29379883
http://dx.doi.org/10.1212/NXG.0000000000000218

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