reference/28871847

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/28871847

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	81
issn	0009-9120
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pageRange	76-81
publicationName	Clinical Biochemistry
startingPage	76
bibliographicCitation	Dahri S, Desviat LR, Pérez B, Leal F, Ugarte M, Chabraoui L. Mutation analysis of phenylketonuria patients from Morocco: high prevalence of mutation G352fsdelG and detection of a novel mutation p.K85X. Clin Biochem. 2010 Jan;43(1-2):76–81. doi: 10.1016/j.clinbiochem.2009.09.018. PMID: 19786003.
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date	201001
identifier	https://doi.org/10.1016/j.clinbiochem.2009.09.018 https://pubmed.ncbi.nlm.nih.gov/19786003
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/2990 https://portal.issn.org/resource/ISSN/0009-9120
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Mutation analysis of phenylketonuria patients from Morocco: High prevalence of mutation G352fsdelG and detection of a novel mutation p.K85X
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Total number of triples: 41.