PLA2G6-associated Dystonia–Parkinsonism: Case Report and Literature Review

BACKGROUND: Phospholipase-associated neurodegeneration (PLAN) caused by PLA2G6 mutations is a recessively inherited disorder with three known phenotypes: the typical infantile onset neuroaxonal dystrophy (INAD); an atypical later onset form (atypical NAD); and the more recently recognized young-onse...

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Detalles Bibliográficos
Autores principales: Karkheiran, Siamak, Shahidi, Gholam Ali, Walker, Ruth H., Paisán-Ruiz, Coro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Columbia University Libraries/Information Services 2015
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4503963/
https://www.ncbi.nlm.nih.gov/pubmed/26196026
http://dx.doi.org/10.7916/D84Q7T4W

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4503963/
https://www.ncbi.nlm.nih.gov/pubmed/26196026
http://dx.doi.org/10.7916/D84Q7T4W

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