Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.
about
NGS Technologies as a Turning Point in Rare Disease Research , Diagnosis and Treatment.The Anatomical Basis for Dystonia: The Motor Network Model.Familial Paroxysmal Kinesigenic Dyskinesia is associated with mutations in the KCNA1 gene.Evolving concepts in the pathogenesis of dystonia.Incidentalome in Neurogenetics: Pathogenic Variant of NSD1 in a Patient With Spinocerebellar Ataxia (SCA).Genetic Dystonia-ataxia Syndromes: Clinical Spectrum, Diagnostic Approach, and Treatment Options
P2860
Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.
description
2017 nî lūn-bûn
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2017年の論文
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2017年論文
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2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
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2017年论文
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name
Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.
@en
Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.
@nl
type
label
Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.
@en
Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.
@nl
prefLabel
Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.
@en
Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.
@nl
P2093
P2860
P1476
Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.
@en
P2093
Cathérine C S Delnooz
Dineke S Verbeek
Esther A R Nibbeling
Hyder A Jinnah
Marina A J Tijssen
Richard J Sinke
Tom J de Koning
P2860
P356
10.1016/J.NEUBIOREV.2017.01.033
P577
2017-01-28T00:00:00Z