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Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations

Detalles Bibliográficos
Autores principales:	Lynch, David S., Loh, Samantha H.Y., Harley, Jasmine, Noyce, Alastair J., Martins, L. Miguel, Wood, Nicholas W., Houlden, Henry, Plun-Favreau, Helene
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer 2017
Materias:	Clinical/Scientific Notes
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610041/ https://www.ncbi.nlm.nih.gov/pubmed/28955727 http://dx.doi.org/10.1212/NXG.0000000000000188

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