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.

Subjects

Subjects :

Cardiomegaly
Humans
Japan
Mutation
Osteochondrodysplasias
Hypertrichosis genetics
KATP Channels genetics

Details

Language :

English

ISSN :

1468-3083

Volume :

34

Issue :

9

Database :

MEDLINE

Journal :

Journal of the European Academy of Dermatology and Venereology : JEADV

Publication Type :

Editorial & Opinion

Accession number :

32215968

Full Text :

https://doi.org/10.1111/jdv.16384