reference/30125668

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/30125668

Outgoing Links

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contentType	Case Reports\|Journal Article\|Research Support, Non-U.S. Gov't
endingPage	1115
issn	0021-9738
issueIdentifier	7
pageRange	1108-1115
publicationName	The Journal of clinical investigation
startingPage	1108
bibliographicCitation	Courtois G, Smahi A, Reichenbach J, Döffinger R, Cancrini C, Bonnet M, Puel A, Chable-Bessia C, Yamaoka S, Feinberg J, Dupuis-Girod S, Bodemer C, Livadiotti S, Novelli F, Rossi P, Fischer A, Israël A, Munnich A, Le Deist F, Casanova JL. A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency. J Clin Invest. 2003 Oct;112(7):1108–15. PMID: 14523047; PMCID: PMC198529.
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date	2003-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1172/jci18714 https://pubmed.ncbi.nlm.nih.gov/14523047 https://pubmed.ncbi.nlm.nih.gov/PMC198529
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency
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Total number of triples: 73.