reference/3804247

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3804247

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contentType	Case Reports\|Journal Article\|Research Support, N.I.H., Extramural\|Research Support, Non-U.S. Gov't
endingPage	2174
issn	0884-0431 1523-4681
issueIdentifier	10
pageRange	2165-2174
publicationName	Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
startingPage	2165
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bibliographicCitation	Mäkitie O, Pereira RC, Kaitila I, Turan S, Bastepe M, Laine T, Kröger H, Cole WG, Jüppner H. Long-term clinical outcome and carrier phenotype in autosomal recessive hypophosphatemia caused by a novel DMP1 mutation. J Bone Miner Res. 2010 Oct;25(10):2165–74. PMID: 20499351; PMCID: PMC3153319.
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date	2010-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/20499351 https://doi.org/10.1002/jbmr.105 https://pubmed.ncbi.nlm.nih.gov/PMC3153319
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Long-term clinical outcome and carrier phenotype in autosomal recessive hypophosphatemia caused by a novel DMP1 mutation
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