reference/27342500

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/27342500

Outgoing Links

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contentType	Case Reports\|Journal Article\|Research Support, Non-U.S. Gov't
endingPage	836
issn	0022-202X
issueIdentifier	5
pageRange	832-836
publicationName	The Journal of investigative dermatology
startingPage	832
bibliographicCitation	Sijbers AM, van Voorst Vader PC, Snoek JW, Raams A, Jaspers NGJ, Kleijer WJ. Homozygous R788W Point Mutation in the XPF Gene of a Patient with Xeroderma Pigmentosum and Late-Onset Neurologic Disease. Journal of Investigative Dermatology. 1998 May;110(5):832–6. doi: 10.1046/j.1523-1747.1998.00171.x.
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date	199805
identifier	https://doi.org/10.1046/j.1523-1747.1998.00171.x https://pubmed.ncbi.nlm.nih.gov/9579555
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/4839 https://portal.issn.org/resource/ISSN/0022-202X
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Homozygous R788W Point Mutation in the XPF Gene of a Patient with Xeroderma Pigmentosum and Late-Onset Neurologic Disease
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Total number of triples: 45.