reference/12509560

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12509560

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endingPage	671
issn	1076-1551 1528-3658
issueIdentifier	10
pageRange	664-671
publicationName	Molecular medicine (Cambridge, Mass.)
startingPage	664
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bibliographicCitation	Solis C, Lopez-Echaniz I, Sefarty-Graneda D, Astrin KH, Desnick RJ. Identification and Expression of Mutations in the Hydroxymethylbilane Synthase Gene Causing Acute Intermittent Porphyria (AIP). Molecular Medicine. 1999 Oct 01;5(10):664–71. doi: 10.1007/bf03401985.
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date	1999-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC2230478 https://doi.org/10.1007/bf03401985 https://pubmed.ncbi.nlm.nih.gov/10602775
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language	English
source	https://scigraph.springernature.com/ https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Identification and Expression of Mutations in the Hydroxymethylbilane Synthase Gene Causing Acute Intermittent Porphyria (AIP)
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Incoming Links

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Total number of triples: 45.