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                                       Details for article 12 of 22 found articles
 
 
  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
Author: Al-Sayed, Moeenaldeen D.
Al-Zaidan, Hamad
Albakheet, AlBandary
Hakami, Hana
Kenana, Rosan
Al-Yafee, Yusra
Al-Dosary, Mazhor
Qari, Alya
Al-Sheddi, Tarfa
Al-Muheiza, Muhammed
Al-Qubbaj, Wafa
Lakmache, Yamina
Al-Hindi, Hindi
Ghaziuddin, Muhammad
Colak, Dilek
Kaya, Namik
Appeared in: The American journal of human genetics
Paging: Volume 93 (2013) nr. 4 pages 6 p.
Year: 2013
Contents:
Publisher: The American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 12 of 22 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands