Rehman, Atteeq U <br/><br/>
Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p.  [electronic resource] 

 -  Human genetics  Dec 2011 
 - 759-65 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1432-1203 
<br/><br/><label>Standard No.: </label>10.1007/s00439-011-1018-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adaptor Proteins, Signal Transducing<br/>Amino Acid Sequence<br/>Base Sequence<br/>Carrier Proteins--genetics<br/>Chromosomes, Human, Pair 19<br/>Female<br/>Frameshift Mutation<br/>Genes, Recessive--genetics<br/>Genetic Linkage<br/>Genetic Loci<br/>Haplotypes<br/>Hearing Loss--genetics<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Mutation, Missense<br/>Pedigree