Genetic Mutation Analysis of Parkinson's Disease Patients Using Multigene Next-Generation Sequencing Panels.
about
Whole-exome sequencing associates novel CSMD1 gene mutations with familial Parkinson diseaseFunctional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease.Whole-Exome Sequencing in Searching for New Variants Associated With the Development of Parkinson's Disease.
P2860
Genetic Mutation Analysis of Parkinson's Disease Patients Using Multigene Next-Generation Sequencing Panels.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Genetic Mutation Analysis of P ...... -Generation Sequencing Panels.
@ast
Genetic Mutation Analysis of P ...... -Generation Sequencing Panels.
@en
type
label
Genetic Mutation Analysis of P ...... -Generation Sequencing Panels.
@ast
Genetic Mutation Analysis of P ...... -Generation Sequencing Panels.
@en
prefLabel
Genetic Mutation Analysis of P ...... -Generation Sequencing Panels.
@ast
Genetic Mutation Analysis of P ...... -Generation Sequencing Panels.
@en
P2093
P2860
P1476
Genetic Mutation Analysis of P ...... t-Generation Sequencing Panels
@en
P2093
Alberto Bergareche
Ana Gorostidi
Javier Ruiz-Martínez
José Félix Martí-Massó
P2860
P2888
P304
P356
10.1007/S40291-016-0216-1
P577
2016-10-01T00:00:00Z