USP1 c.292-271A>G

Variant ID: 1-62907595-A-G

NM_003368.4(USP1):c.292-271A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Mutations in the ANGPTL3 gene and familial combined hypolipidemia: a clinical and biochemical characterization.

The Journal Of Clinical Endocrinology And Metabolism
Minicocci, Ilenia I; Montali, Anna A; Robciuc, Marius Robert MR; Quagliarini, Fabiana F; Censi, Vincenzo V; Labbadia, Giancarlo G; Gabiati, Claudia C; Pigna, Giovanni G; Sepe, Maria Laura ML; Pannozzo, Fabio F; Lütjohann, Dieter D; Fazio, Sergio S; Jauhiainen, Matti M; Ehnholm, Christian C; Arca, Marcello M
Publication Date: 2012-07

Variant appearance in text: rs656297
PubMed Link: 22659251
Variant Present in the following documents:
  • Main text
View BVdb publication page