reference/16854296

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16854296

Outgoing Links

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issn	1471-2350
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pageRange	33-
publicationName	BMC Medical Genetics
startingPage	33
bibliographicCitation	Choi R, Park H, Kang B, Choi SY, Ki C, Lee S, Kim J, Song J, Choe YH. PHKA2 mutation spectrum in Korean patients with glycogen storage disease type IX: prevalence of deletion mutations. BMC Medical Genomics. 2016 Apr 21;17(1):33. doi: 10.1186/s12881-016-0295-1.
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date	2016-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/27103379 https://doi.org/10.1186/s12881-016-0295-1 https://pubmed.ncbi.nlm.nih.gov/PMC4839068
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language	English
source	https://scigraph.springernature.com/ https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	PHKA2 mutation spectrum in Korean patients with glycogen storage disease type IX: prevalence of deletion mutations
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Total number of triples: 42.