Heathcote, K <br/><br/>
A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350).  [electronic resource] 

 -  Journal of medical genetics  Jan 2000 
 - 50-1 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-2593 
<br/><br/><label>Standard No.: </label>10.1136/jmg.37.1.50  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Connexin 26<br/>Connexins--genetics<br/>Exons<br/>Female<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Keratoderma, Palmoplantar--genetics<br/>Male<br/>Mutation, Missense<br/>Pedigree<br/>Polymorphism, Single-Stranded Conformational<br/>Syndrome