R32W variant in Connexin 31: mutation or polymorphism for deafness and skin disease?

Authors	N López-Bigas, R Rabionet, M L Arbonés, X Estivill
Journal	European journal of human genetics : EJHG (Eur J Hum Genet) Vol. 9 Issue 1 Pg. 70 (Jan 2001) ISSN: 1018-4813 [Print] England
PMID	11175305 (Publication Type: Comment, Letter, Research Support, Non-U.S. Gov't)
Chemical References	Connexins GJB3 protein, human
Topics	Amino Acid Substitution Connexins (genetics) Deafness (genetics) Family Health Female Humans Male Mutation Polymorphism, Genetic Skin Diseases (genetics)

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