PEX7 Mutations Cause Congenital Cataract Retinopathy and Late-Onset Ataxia and Cognitive Impairment: Report of Two Siblings and Review of the Literature

Detalles Bibliográficos
Autores principales: Nanetti, Lorenzo, Pensato, Viviana, Leoni, Valerio, Rizzetto, Manuela, Caccia, Claudio, Taroni, Franco, Mariotti, Caterina, Gellera, Cinzia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2015
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387488/
https://www.ncbi.nlm.nih.gov/pubmed/25851898
http://dx.doi.org/10.3988/jcn.2015.11.2.197

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387488/
https://www.ncbi.nlm.nih.gov/pubmed/25851898
http://dx.doi.org/10.3988/jcn.2015.11.2.197

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