The curious case of phenocopies in families with genetic Parkinson's disease.
about
Pharmacological rescue of mitochondrial deficits in iPSC-derived neural cells from patients with familial Parkinson's disease.Medical genomics: The intricate path from genetic variant identification to clinical interpretationGenetics of Parkinson's diseaseMissense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremorDNAJC13 mutations in Parkinson diseaseExome sequencing: a transformative technologyOlfactory identification in LRRK2 G2019S mutation carriers: a relevant marker?Whole-Exome Sequencing in Familial Parkinson Disease.The neuropathology of genetic Parkinson's disease.Genes and functional GI disorders: from casual to causal relationship.Genetics and genomics of Parkinson's disease.Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias.Common genetic etiology between "multiple sclerosis-like" single-gene disorders and familial multiple sclerosis.
P2860
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P2860
The curious case of phenocopies in families with genetic Parkinson's disease.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
The curious case of phenocopies in families with genetic Parkinson's disease.
@ast
The curious case of phenocopies in families with genetic Parkinson's disease.
@en
type
label
The curious case of phenocopies in families with genetic Parkinson's disease.
@ast
The curious case of phenocopies in families with genetic Parkinson's disease.
@en
prefLabel
The curious case of phenocopies in families with genetic Parkinson's disease.
@ast
The curious case of phenocopies in families with genetic Parkinson's disease.
@en
P2860
P50
P356
P1433
P1476
The curious case of phenocopies in families with genetic Parkinson's disease.
@en
P2093
Rosalind Chuang
P2860
P304
P356
10.1002/MDS.23853
P407
P577
2011-07-06T00:00:00Z