Mutations in <em>NALCN</em> Cause an Autosomal-Recessive Syndrome with Severe Hypotonia,Speech Impairment,and Cognitive Delay期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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

Authors:	Moeenaldeen D. Al-Sayed,Hamad Al-Zaidan,AlBandary Albakheet,Hana Hakami,Rosan Kenana,Yusra Al-Yafee,Mazhor Al-Dosary,Alya Qari,Tarfa Al-Sheddi,Muhammed Al-Muheiza,Wafa Al-Qubbaj,Yamina Lakmache,Hindi Al-Hindi,Muhammad Ghaziuddin,Dilek Colak,Namik Kaya

Affiliation:	¹ Department of Medical Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia;² Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia;³ Department of Biostatistics, Epidemiology, and Scientific Computing, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia;⁴ Department of Neurosciences, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia;⁵ Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia;⁶ Department of Mental Health, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia

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