reference/661028

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/661028

Outgoing Links

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contentType	Journal Article
issn	2324-9269
issueIdentifier	4
pageRange	e1577-
publicationName	Molecular genetics & genomic medicine
startingPage	e1577
bibliographicCitation	Xie F, Lei L, Cai B, Gan L, Gao Y, Liu X, Zhou L, Jiang J. Clinical manifestation and phenotypic analysis of novel gene mutation in 28 Chinese children with hereditary spherocytosis. Mol Genet Genomic Med. 2021 Apr;9(4):e1577. PMID: 33620149; PMCID: PMC8123760.
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date	2021-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC8123760 https://doi.org/10.1002/mgg3.1577 https://pubmed.ncbi.nlm.nih.gov/33620149
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Clinical manifestation and phenotypic analysis of novel gene mutation in 28 Chinese children with hereditary spherocytosis
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Total number of triples: 41.