Label Value
DOI 10.1038/jhg.2016.1
TITLE De novo KCNH1 mutations in four patients with syndromic developmental delay, hypotonia and seizures
TYPE article
PUBLICATION DATE
Service Status Date Last Checked
Scopus Yes 2018-02-12T11:02:06.401080
Web of Science Yes 2018-04-08T10:47:51.355909
Compendex No 2020-12-23T16:51:43.992306