Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay

Title
Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay
Authors
Keywords
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Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 93, Issue 4, Pages 721-726
Publisher
Elsevier BV
Online
2013-09-27
DOI
10.1016/j.ajhg.2013.08.001

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