reference/12582541

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12582541

Outgoing Links

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endingPage	2723
issn	1460-2083 0964-6906
issueIdentifier	21
pageRange	2709-2723
publicationName	Human Molecular Genetics
startingPage	2709
bibliographicCitation	Matsuda J, Kido M, Tadano-Aritomi K, Ishizuka I, Tominaga K, Toida K, Takeda E, Suzuki K, Kuroda Y. Mutation in saposin D domain of sphingolipid activator protein gene causes urinary system defects and cerebellar Purkinje cell degeneration with accumulation of hydroxy fatty acid-containing ceramide in mouse. Hum Mol Genet. 2004 Nov 01;13(21):2709–23. doi: 10.1093/hmg/ddh281. PMID: 15345707.
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date	2004-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1093/hmg/ddh281 https://pubmed.ncbi.nlm.nih.gov/15345707
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Mutation in saposin D domain of sphingolipid activator protein gene causes urinary system defects and cerebellar Purkinje cell degeneration with accumulation of hydroxy fatty acid-containing ceramide in mouse
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