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Midnolin is a confirmed genetic risk factor for Parkinson’s disease

OBJECTIVE: Genetic analysis of patients with familial Parkinson’s disease (PD) identified many causative genes. However, the majority of PD cases are sporadic, and the mechanisms of onset still remain unclear. Previously, we found that Midnolin (MIDN) is associated with PD in a Yamagata (Japan) coho...

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Bibliografiske detaljer
Udgivet i:Ann Clin Transl Neurol
Main Authors: Obara, Yutaro, Sato, Hidenori, Nakayama, Takahiro, Kato, Takeo, Ishii, Kuniaki
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2019
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6856597/
https://ncbi.nlm.nih.gov/pubmed/31588691
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.50914
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