Referenced in: none

Automatically associated channels: Kir1.1 , Kir4.1 , TRP

Title: Lack of significant association between mutations of KCNJ10 or FOXI1 and SLC26A4 mutations in Pendred syndrome/enlarged vestibular aqueducts.

Authors: Priya Landa, Ann-Marie Differ, Kaukab Rajput, Lucy Jenkins, Maria Bitner-Glindzicz

Journal, date & volume: BMC Med. Genet., 2013 , 14, 85

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/23965030

Abstract