reference/7880221

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7880221

Outgoing Links

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endingPage	1257
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issueIdentifier	5
pageRange	1250-1257
publicationName	The Journal of clinical investigation
startingPage	1250
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bibliographicCitation	Gensure RC, Mäkitie O, Barclay C, Chan C, Depalma SR, Bastepe M, Abuzahra H, Couper R, Mundlos S, Sillence D, Ala Kokko L, Seidman JG, Cole WG, Jüppner H. A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders. J Clin Invest. 2005 May;115(5):1250–7. PMID: 15864348; PMCID: PMC1087158.
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date	2005-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC1087158 https://doi.org/10.1172/jci22760 https://pubmed.ncbi.nlm.nih.gov/15864348
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders
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