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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Detaylı Bibliyografya
Yayımlandı:Tremor Other Hyperkinet Mov (N Y)
Asıl Yazarlar: Karkheiran, Siamak, Shahidi, Gholam Ali, Walker, Ruth H., Paisán-Ruiz, Coro
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Columbia University Libraries/Information Services 2015
Konular:
Case Reports
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4503963/
https://ncbi.nlm.nih.gov/pubmed/26196026
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7916/D84Q7T4W
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