Lv1
60 积分 2023-08-31 加入
A novel homozygous COX6A1 variant causes axonal charcot-marie-tooth disease, developmental delays and mitochondrial dysfunction
7个月前
已关闭
A Homozygous PTRHD1 Missense Variant (p.Arg122Gln) in an Individual with Intellectual Disability, Generalized Epilepsy, and Juvenile Parkinsonism
7个月前
已完结
The PTRHD1 Mutation in Intellectual Disability
7个月前
已关闭
Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes
7个月前
已完结
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
7个月前
已完结
Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1
7个月前
已完结
Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease
7个月前
已完结
Towards biomarker-based diagnosis of Parkinson disease
7个月前
已完结
Towards a Biological Definition of Parkinson’s Disease
7个月前
已关闭
Diagnosis and Treatment of Parkinson Disease
7个月前
已完结
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