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

Moeenaldeen AlSayed, Hamad Alzaidan, Albandary AlBakheet, Hana Hakami, Rosan Kenana, Yusra Alyafee, Mazhor Aldosary, Alya Qari, Tarfa Al‐Sheddi, Muhammed Al-Muheiza,

The American Journal of Human Genetics · 2013 · 120 citations · 12 references

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