Hmani-Aifa, Mounira <br/><br/>
Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.  [electronic resource] 

 -  European journal of human genetics : EJHG  Apr 2009 
 - 474-82 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>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2008.167  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Base Sequence<br/>Consanguinity<br/>Cyclic Nucleotide Phosphodiesterases, Type 6--genetics<br/>Family<br/>Hearing Loss--congenital<br/>Humans<br/>Molecular Sequence Data<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Receptors, G-Protein-Coupled--genetics<br/>Retinal Degeneration--genetics<br/>Retinitis Pigmentosa--genetics<br/>Tunisia<br/>Usher Syndromes--genetics