CP c.1864+113C>T

Variant ID: 3-148905726-G-A

NM_000096.3(CP):c.1864+113C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Analysis of nucleotide variations in genes of iron management in patients of Parkinson's disease and other movement disorders.

Parkinson'S Disease
Castiglioni, Emanuela E; Finazzi, Dario D; Goldwurm, Stefano S; Pezzoli, Gianni G; Forni, Gianluca G; Girelli, Domenico D; Maccarinelli, Federica F; Poli, Maura M; Ferrari, Maurizio M; Cremonesi, Laura L; Arosio, Paolo P
Publication Date: 2010-10-17

Variant appearance in text: rs35516209
PubMed Link: 20981230
Variant Present in the following documents:
  • Main text
  • PD2011-827693.pdf
View BVdb publication page