VPS35 and DNAJC13 disease-causing variants in essential tremor

Exome-sequencing analyses have identified vacuolar protein sorting 35 homolog (VPS35) and DnaJ (Hsp40) homolog, subfamily C, member 13 (DNAJC13) harboring disease-causing variants for Parkinson disease (PD). Owing to the suggested clinical, pathological and genetic overlap between PD and essential t...

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Dades bibliogràfiques
Publicat a:Eur J Hum Genet
Autors principals: Rajput, Alex, Ross, Jay P, Bernales, Cecily Q, Rayaprolu, Sruti, Soto-Ortolaza, Alexandra I, Ross, Owen A, van Gerpen, Jay, Uitti, Ryan J, Wszolek, Zbigniew K, Rajput, Ali H, Vilariño-Güell, Carles
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group 2015
Matèries:
Short Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4795043/
https://ncbi.nlm.nih.gov/pubmed/25118025
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2014.164
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