reference/23063624

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/23063624

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bibliographicCitation	Chelban V, Patel N, Vandrovcova J, Zanetti MN, Lynch DS, Ryten M, Botía JA, Bello O, Tribollet E, Efthymiou S, Davagnanam I; SYNAPSE Study Group, Bashiri FA, Wood NW, Rothman JE, Alkuraya FS, Houlden H. Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination. Am J Hum Genet. 2017 Jun 01;100(6):969–77. PMID: 28575651; PMCID: PMC5473715.
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date	2017-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC5473715 https://pubmed.ncbi.nlm.nih.gov/28575651 https://doi.org/10.1016/j.ajhg.2017.05.009
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language	English
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title	Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination
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