Cuevas, J M <br/><br/>
Identification of three novel mutations in the MYO7A gene.  [electronic resource] 

 -  Human mutation  Aug 1999 
 - 181 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/(SICI)1098-1004(1999)14:2<181::AID-HUMU11>3.0.CO;2-3  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Chromosomes, Human, Pair 11<br/>Dyneins<br/>Female<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Male<br/>Mutation<br/>Myosin VIIa<br/>Myosins--genetics<br/>Pedigree<br/>Phenotype<br/>Polymorphism, Single-Stranded Conformational<br/>Retinitis Pigmentosa--genetics<br/>Syndrome