Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay (Q37217068)
scientific article published on 26 September 2013
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| English | Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay |
scientific article published on 26 September 2013 |
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Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay (English)
1 reference
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
26 September 2013
1 reference