reference/23439619

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/23439619

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bibliographicCitation	Cantagrel V, Silhavy JL, Bielas SL, Swistun D, Marsh SE, Bertrand JY, Audollent S, Attié-Bitach T, Holden KR, Dobyns WB, Traver D, Al-Gazali L, Ali BR, Lindner TH, Caspary T, Otto EA, Hildebrandt F, Glass IA, Logan CV, Johnson CA, Bennett C, Brancati F; International Joubert Syndrome Related Disorders Study Group, Valente EM, Woods CG, Gleeson JG. Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome. Am J Hum Genet. 2008 Aug;83(2):170–9. PMID: 18674751; PMCID: PMC2495072.
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date	200808
identifier	https://pubmed.ncbi.nlm.nih.gov/18674751 https://pubmed.ncbi.nlm.nih.gov/PMC2495072 https://doi.org/10.1016/j.ajhg.2008.06.023
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome
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