reference/18907949

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18907949

Outgoing Links

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endingPage	1946
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pageRange	1931-1946
publicationName	Human Molecular Genetics
startingPage	1931
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bibliographicCitation	Festa BP, Berquez M, Gassama A, Amrein I, Ismail HM, Samardzija M, Staiano L, Luciani A, Grimm C, Nussbaum RL, De Matteis MA, Dorchies OM, Scapozza L, Wolfer DP, Devuyst O. OCRL deficiency impairs endolysosomal function in a humanized mouse model for Lowe syndrome and Dent disease. Hum Mol Genet. 2019 Jun 15;28(12):1931–46. PMID: 30590522; PMCID: PMC6548226.
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date	2018-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC6548226 https://doi.org/10.1093/hmg/ddy449 https://pubmed.ncbi.nlm.nih.gov/30590522
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	OCRL deficiency impairs endolysosomal function in a humanized mouse model for Lowe syndrome and Dent disease
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