Chihara, M <br/><br/>
A novel mutation in the KCNJ8 gene encoding the Kir6.1 subunit of an ATP-sensitive potassium channel in a Japanese patient with Cantú syndrome.  [electronic resource] 

 -  Journal of the European Academy of Dermatology and Venereology : JEADV  Sep 2020 
 - e476-e478 p.  digital 
<br/><br/> Publication Type: Letter 
<br/><br/><label>ISSN: </label>1468-3083 
<br/><br/><label>Standard No.: </label>10.1111/jdv.16384  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cardiomegaly<br/>Humans<br/>Hypertrichosis--genetics<br/>Japan<br/>KATP Channels--genetics<br/>Mutation<br/>Osteochondrodysplasias