reference/19006874

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/19006874

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bibliographicCitation	Cortese A, Simone R, Sullivan R, Vandrovcova J, Tariq H, Yau WY, Humphrey J, Jaunmuktane Z, Sivakumar P, Polke J, Ilyas M, Tribollet E, Tomaselli PJ, Devigili G, Callegari I, Versino M, Salpietro V, Efthymiou S, Kaski D, Wood NW, Andrade NS, Buglo E, Rebelo A, Rossor AM, Bronstein A, Fratta P, Marques WJ, Züchner S, Reilly MM, Houlden H. Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia. Nature Genetics. 2019 Mar 29;51(4):649–58. doi: 10.1038/s41588-019-0372-4.
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date	2019-03-29^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC6709527 https://doi.org/10.1038/s41588-019-0372-4 https://pubmed.ncbi.nlm.nih.gov/30926972
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://scigraph.springernature.com/ https://www.crossref.org/
title	Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia
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