reference/6731591

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6731591

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publicationName	Clinica chimica acta; international journal of clinical chemistry
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bibliographicCitation	Ge MM, Hu L, Li Z, Cheng G, Yan K, Kong Y, Wang H, Yang L, Zhou W. Novel compound heterozygous mutations in the PEX1 gene in two Chinese newborns with Zellweger syndrome based on whole exome sequencing. Clin Chim Acta. 2017 Jul;470():24–8. doi: 10.1016/j.cca.2017.04.016. PMID: 28432012.
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date	201707
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Novel compound heterozygous mutations in the PEX1 gene in two Chinese newborns with Zellweger syndrome based on whole exome sequencing
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