Aberrant transcriptional networks in step-wise neurogenesis of paroxysmal kinesigenic dyskinesia-induced pluripotent stem cells

Paroxysmal kinesigenic dyskinesia (PKD) is an episodic movement disorder with autosomal-dominant inheritance and marked variability in clinical manifestations. Proline-rich transmembrane protein 2 (PRRT2) has been identified as a causative gene of PKD, but the molecular mechanism underlying the path...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Oncotarget
Main Authors: Li, Chun, Ma, Yu, Zhang, Kunshan, Gu, Junjie, Tang, Fan, Chen, Shengdi, Cao, Li, Li, Siguang, Jin, Ying
Format: Artigo
Jezik:Inglês
Izdano: Impact Journals LLC 2016
Teme:
Research Paper
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5288209/
https://ncbi.nlm.nih.gov/pubmed/27449084
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.10680
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