reference/2005961

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/2005961

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startingPage	e3279
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bibliographicCitation	Khan MI, Latif M, Saif M, Ahmad H, Khan AU, Naseer MI, Hussain HMJ, Jelani M. Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family. The Journal of Gene Medicine. 2020 Oct 27;23(1). doi: 10.1002/jgm.3279.
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date	2020-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1002/jgm.3279 https://pubmed.ncbi.nlm.nih.gov/32989887
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family
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