CUX1 c.4384C>T ;(p.L1462F)

Variant ID: 7-101892188-C-T

NM_181552.3(CUX1):c.4384C>T;(p.L1462F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Prioritization of candidate genes for a South African family with Parkinson's disease using in-silico tools.

Plos One
Sebate, Boiketlo B; Cuttler, Katelyn K; Cloete, Ruben R; Britz, Marcell M; Christoffels, Alan A; Williams, Monique M; Carr, Jonathan J; Bardien, Soraya S
Publication Date: 2021

Variant appearance in text: CUX1: 4384C>T
PubMed Link: 33770142
Variant Present in the following documents:
  • pone.0249324.s003.xlsx, sheet 1
View BVdb publication page