López-Bigas, N <br/><br/>
R32W variant in Connexin 31: mutation or polymorphism for deafness and skin disease?  [electronic resource] 

 -  European journal of human genetics : EJHG  Jan 2001 
 - 70 p.  digital 
<br/><br/> Publication Type: Comment; Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1018-4813 
<br/><br/><label>Standard No.: </label>10.1038/sj.ejhg.5200569  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Connexins--genetics<br/>Deafness--genetics<br/>Family Health<br/>Female<br/>Humans<br/>Male<br/>Mutation<br/>Polymorphism, Genetic<br/>Skin Diseases--genetics