Chishti, Muhammad S <br/><br/>
Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families.  [electronic resource] 

 -  Journal of human genetics  2008 
 - 101-105 p.  digital 
<br/><br/> Publication Type: Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1434-5161 
<br/><br/><label>Standard No.: </label>10.1007/s10038-007-0209-3  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 2--genetics<br/>Consanguinity<br/>DNA Mutational Analysis<br/>Female<br/>Genes, Recessive--genetics<br/>Genetic Linkage<br/>Genotype<br/>Hearing Loss--genetics<br/>Humans<br/>Lod Score<br/>MARVEL Domain Containing 2 Protein<br/>Male<br/>Membrane Proteins--genetics<br/>Mutation--genetics<br/>Pakistan<br/>Pedigree<br/>Polymerase Chain Reaction<br/>RNA Splice Sites--genetics<br/>Tight Junctions