Hogewind, Barend F T <br/><br/>
Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1.  [electronic resource] 

 -  Molecular vision  Jan 2010 
 - 26-35 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1090-0535 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged, 80 and over<br/>Amino Acid Sequence<br/>Base Sequence<br/>Conserved Sequence<br/>DNA Mutational Analysis<br/>Diabetes Mellitus--genetics<br/>Evolution, Molecular<br/>Family<br/>Female<br/>Genes, Dominant--genetics<br/>Genetic Association Studies<br/>Genetic Predisposition to Disease<br/>Hearing Loss, Sensorineural--complications<br/>Hearing Tests<br/>Humans<br/>Male<br/>Membrane Proteins--chemistry<br/>Middle Aged<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Ocular Physiological Phenomena<br/>Optic Nerve Diseases--complications<br/>Pedigree<br/>Phenotype<br/>Young Adult