Lv1
50 积分 2023-08-31 加入
A Homozygous PTRHD1 Missense Variant (p.Arg122Gln) in an Individual with Intellectual Disability, Generalized Epilepsy, and Juvenile Parkinsonism
1天前
已完结
The PTRHD1 Mutation in Intellectual Disability
1天前
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
4天前
已完结
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
4天前
已完结
Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1
5天前
已完结
Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease
10天前
已完结
Towards biomarker-based diagnosis of Parkinson disease
11天前
已完结
Towards a Biological Definition of Parkinson’s Disease
11天前
已关闭
Diagnosis and Treatment of Parkinson Disease
15天前
已完结
Sphingolipids in the Pathogenesis of Parkinson’s Disease and Parkinsonism
18天前
已完结
皖公网安备34019202002308
