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pubmed-article:21050253 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:21050253 | lifeskim:mentions | umls-concept:C0599755 | lld:lifeskim |
pubmed-article:21050253 | lifeskim:mentions | umls-concept:C1704375 | lld:lifeskim |
pubmed-article:21050253 | lifeskim:mentions | umls-concept:C1418526 | lld:lifeskim |
pubmed-article:21050253 | lifeskim:mentions | umls-concept:C1414605 | lld:lifeskim |
pubmed-article:21050253 | lifeskim:mentions | umls-concept:C1414084 | lld:lifeskim |
pubmed-article:21050253 | lifeskim:mentions | umls-concept:C1422784 | lld:lifeskim |
pubmed-article:21050253 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
pubmed-article:21050253 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:21050253 | pubmed:dateCreated | 2011-2-8 | lld:pubmed |
pubmed-article:21050253 | pubmed:abstractText | X-linked hypophosphatemic rickets, autosomal dominant hypophosphatemic rickets and autosomal recessive hypophosphatemic rickets make up a group of renal phosphate wasting disorders with common clinical and biochemical characteristics. These three types of rickets are related to mutations in PHEX, FGF23 and dentin matrix protein 1 (DMP1), respectively. | lld:pubmed |
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pubmed-article:21050253 | pubmed:language | eng | lld:pubmed |
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pubmed-article:21050253 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:21050253 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:21050253 | pubmed:month | Mar | lld:pubmed |
pubmed-article:21050253 | pubmed:issn | 1365-2265 | lld:pubmed |
pubmed-article:21050253 | pubmed:author | pubmed-author:BrosnanPatric... | lld:pubmed |
pubmed-article:21050253 | pubmed:author | pubmed-author:NorthrupHopeH | lld:pubmed |
pubmed-article:21050253 | pubmed:author | pubmed-author:DominguezBarb... | lld:pubmed |
pubmed-article:21050253 | pubmed:author | pubmed-author:RuppeMary DMD | lld:pubmed |
pubmed-article:21050253 | pubmed:author | pubmed-author:AuKit SingKS | lld:pubmed |
pubmed-article:21050253 | pubmed:author | pubmed-author:TranPhong XPX | lld:pubmed |
pubmed-article:21050253 | pubmed:copyrightInfo | © 2011 Blackwell Publishing Ltd. | lld:pubmed |
pubmed-article:21050253 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:21050253 | pubmed:volume | 74 | lld:pubmed |
pubmed-article:21050253 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:21050253 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:21050253 | pubmed:pagination | 312-8 | lld:pubmed |
pubmed-article:21050253 | pubmed:dateRevised | 2011-9-26 | lld:pubmed |
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pubmed-article:21050253 | pubmed:year | 2011 | lld:pubmed |
pubmed-article:21050253 | pubmed:articleTitle | Mutational analysis of PHEX, FGF23 and DMP1 in a cohort of patients with hypophosphatemic rickets. | lld:pubmed |
pubmed-article:21050253 | pubmed:affiliation | Department of Medicine, University of Texas Health Science Center at Houston, TX 77030, USA. mary.ruppe@uth.tmc.edu | lld:pubmed |
pubmed-article:21050253 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:21050253 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:21050253 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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