Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations
Volume
3
Pagination
e188 - e188
DOI
10.1212/NXG.0000000000000188
Journal
Neurology Genetics
Issue
Metadata
Show full item recordAuthors
Lynch, DS; Loh, SHY; Harley, J; Noyce, AJ; Martins, LM; Wood, NW; Houlden, H; Plun-Favreau, HCollections
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