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Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay |
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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: |
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Publisher: |
The American Society of Human Genetics |
Source file: |
Elektronische Wetenschappelijke Tijdschriften |
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