Nomura, K <br/><br/>
A keratin K10 gene mutation in a Japanese patient with epidermolytic hyperkeratosis.  [electronic resource] 

 -  The Japanese journal of human genetics  Mar 1997 
 - 217-23 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0916-8478 
<br/><br/><label>Standard No.: </label>10.1007/BF02766925  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Child, Preschool<br/>Female<br/>Genes--genetics<br/>Humans<br/>Hyperkeratosis, Epidermolytic--genetics<br/>Japan<br/>Keratins--genetics<br/>Molecular Sequence Data<br/>Nucleic Acid Heteroduplexes--analysis<br/>Point Mutation<br/>Sequence Homology, Amino Acid