reference/33833235

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/33833235

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issn	2324-9269
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pageRange	e1434-
publicationName	Molecular Genetics & Genomic Medicine
startingPage	e1434
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bibliographicCitation	Yuan H, Yuan H, Wang Q, Ye W, Yao R, Xu W, Liu Y. Two novel KCNA1 variants identified in two unrelated Chinese families affected by episodic ataxia type 1 and neurodevelopmental disorders. Mol Genet Genomic Med. 2020 Oct;8(10):e1434. PMID: 32705822; PMCID: PMC7549609.
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date	2020-07-23^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1002/mgg3.1434 https://pubmed.ncbi.nlm.nih.gov/PMC7549609 https://pubmed.ncbi.nlm.nih.gov/32705822
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Two novel KCNA1 variants identified in two unrelated Chinese families affected by episodic ataxia type 1 and neurodevelopmental disorders
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