ReviewJournal of human genetics2016
De novo KCNH1 mutations in four patients with syndromic developmental delay, hypotonia and seizures.
Ryoko Fukai et al.PubMed ↗Publisher ↗
No numbers read from the abstract.
25 papers cite it
this papercites it
ReviewJournal of human genetics2016
Ryoko Fukai et al.PubMed ↗Publisher ↗
No numbers read from the abstract.