reference/8299967

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8299967

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endingPage	358
issn	1432-1203 0340-6717
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pageRange	352-358
publicationName	Human Genetics
startingPage	352
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bibliographicCitation	Natt E, Westphal EM, Toth-Fejel SE, Magenis RE, Buist NR, Rettenmeier R, Scherer G. Inherited and de novo deletion of the tyrosine aminotransferase gene locus at 16q22.1----q22.3 in a patient with tyrosinemia type II. Hum Genet. 1987 Dec;77(4):352–8. doi: 10.1007/bf00291426. PMID: 2891604.
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date	198712
identifier	https://pubmed.ncbi.nlm.nih.gov/2891604 https://doi.org/10.1007/bf00291426
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://scigraph.springernature.com/ https://www.crossref.org/
title	Inherited and de novo deletion of the tyrosine aminotransferase gene locus at 16q22.1----q22.3 in a patient with tyrosinemia type II
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