reference/6679509

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endingPage	215
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publicationName	The American Journal of Human Genetics
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bibliographicCitation	Shamseldin H, Faqeih E, Alasmari A, Zaki M, Gleeson J, Alkuraya F. Mutations in UNC80, Encoding Part of the UNC79-UNC80-NALCN Channel Complex, Cause Autosomal-Recessive Severe Infantile Encephalopathy. The American Journal of Human Genetics. 2016 Jan;98(1):210–5. doi: 10.1016/j.ajhg.2015.11.013.
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date	2016-01-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/26708753 https://doi.org/10.1016/j.ajhg.2015.11.013 https://pubmed.ncbi.nlm.nih.gov/PMC4716667
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Mutations in UNC80, Encoding Part of the UNC79-UNC80-NALCN Channel Complex, Cause Autosomal-Recessive Severe Infantile Encephalopathy
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