LRRK2 c.81G>T ;(p.Q27H)

Variant ID: 12-40619014-G-T

NM_198578.3(LRRK2):c.81G>T;(p.Q27H)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Risk of Parkinson disease in carriers of parkin mutations: estimation using the kin-cohort method.

Archives Of Neurology
Wang, Yuanjia Y; Clark, Lorraine N LN; Louis, Elan D ED; Mejia-Santana, Helen H; Harris, Juliette J; Cote, Lucien J LJ; Waters, Cheryl C; Andrews, Howard H; Ford, Blair B; Frucht, Steven S; Fahn, Stanley S; Ottman, Ruth R; Rabinowitz, Daniel D; Marder, Karen K
Publication Date: 2008-04

Variant appearance in text: LRRK2: 81G>T
PubMed Link: 18413468
Variant Present in the following documents:
  • Main text
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