reference/31171546

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/31171546

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
issn	2045-2322
issueIdentifier	1
pageRange	13337-
publicationName	Scientific Reports
startingPage	13337
bibliographicCitation	Fareed M, Makkar V, Angral R, Afzal M, Singh G. Whole-exome sequencing reveals a novel homozygous mutation in the COQ8B gene associated with nephrotic syndrome. Scientific Reports. 2021 Jun 25;11(1):13337. doi: 10.1038/s41598-021-92023-3.
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date	2021-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1038/s41598-021-92023-3 https://pubmed.ncbi.nlm.nih.gov/34172776 https://pubmed.ncbi.nlm.nih.gov/PMC8233304
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://scigraph.springernature.com/ https://www.crossref.org/
title	Whole-exome sequencing reveals a novel homozygous mutation in the COQ8B gene associated with nephrotic syndrome
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