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Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay |
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Titel: |
Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay |
Auteur: |
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 |
Verschenen in: |
The American journal of human genetics |
Paginering: |
Jaargang 93 (2013) nr. 4 pagina's 6 p. |
Jaar: |
2013 |
Inhoud: |
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Uitgever: |
The American Society of Human Genetics |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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