reference/2282697

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/2282697

Outgoing Links

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contentType	Clinical Trial\|Journal Article
endingPage	23
issn	1573-2665 0141-8955
issueIdentifier	1
pageRange	17-23
publicationName	Journal of Inherited Metabolic Disease
startingPage	17
bibliographicCitation	Uyguner O, Goicoechea de Jorge E, Cefle A, Baykal T, Kayserili H, Cefle K, Demirkol M, Yuksel-Apak M, Rodriguez de Córdoba S, Wollnik B. Molecular analyses of the HGO gene mutations in Turkish alkaptonuria patients suggest that the R58fs mutation originated from central Asia and was spread throughout Europe and Anatolia by human migrations. J Inherit Metab Dis. 2003;26(1):17–23. doi: 10.1023/a:1024063126954. PMID: 12872836.
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date	200307
identifier	https://doi.org/10.1023/a:1024063126954 https://pubmed.ncbi.nlm.nih.gov/12872836
isPartOf	https://portal.issn.org/resource/ISSN/0141-8955 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/5452 https://portal.issn.org/resource/ISSN/1573-2665
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Molecular analyses of the HGO gene mutations in Turkish alkaptonuria patients suggest that the R58fs mutation originated from Central Asia and was spread throughout Europe and Anatolia by human migrations
discusses	http://id.nlm.nih.gov/mesh/M0015676 http://id.nlm.nih.gov/mesh/M0464092 http://id.nlm.nih.gov/mesh/M0076145 http://id.nlm.nih.gov/mesh/M0006644
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Incoming Links

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Total number of triples: 42.