PLPP3 c.139+18787G>A

Variant ID: 1-57025764-C-T

NM_003713.4(PLPP3):c.139+18787G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.

American Journal Of Human Genetics
Oliveira, Sofia A SA; Li, Yi-Ju YJ; Noureddine, Maher A MA; Zuchner, Stephan S; Qin, Xuejun X; Pericak-Vance, Margaret A MA; Vance, Jeffery M JM
Publication Date: 2005-08

Variant appearance in text: rs1777284
PubMed Link: 15986317
Variant Present in the following documents:
  • Main text
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