reference/24375492

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/24375492

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publicationName	Molecular Medicine Reports
startingPage	5059
bibliographicCitation	Wang J, Qi D, Yang J, Zhang D, Wang Q, Ju X, Zhong X. Novel compound heterozygous PKHD1 mutations cause autosomal recessive polycystic kidney disease in a Han Chinese family. Mol Med Rep. 2019 Dec;20(6):5059–63. PMID: 31638247; PMCID: PMC6854546.
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date	2019-10-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/31638247 https://doi.org/10.3892/mmr.2019.10738 https://pubmed.ncbi.nlm.nih.gov/PMC6854546
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Novel compound heterozygous PKHD1 mutations cause autosomal recessive polycystic kidney disease in a Han Chinese family
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Total number of triples: 51.