Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations.
about
Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
@zh
2017年论文
@zh-cn
name
Nonsyndromic Parkinson disease ...... atrophy due to OPA1 mutations.
@en
type
label
Nonsyndromic Parkinson disease ...... atrophy due to OPA1 mutations.
@en
prefLabel
Nonsyndromic Parkinson disease ...... atrophy due to OPA1 mutations.
@en
P2093
P2860
P1433
P1476
Nonsyndromic Parkinson disease ...... atrophy due to OPA1 mutations
@en
P2093
David S Lynch
Helene Plun-Favreau
Henry Houlden
Jasmine Harley
L Miguel Martins
Nicholas W Wood
Samantha H Y Loh
P2860
P356
10.1212/NXG.0000000000000188
P577
2017-09-22T00:00:00Z