reference/23547744

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publicationName	The American Journal of Human Genetics
startingPage	760
bibliographicCitation	Dirami T, Rode B, Jollivet M, Da Silva N, Escalier D, Gaitch N, Norez C, Tuffery P, Wolf J, Becq F, Ray P, Dulioust E, Gacon G, Bienvenu T, Touré A. Missense Mutations in SLC26A8, Encoding a Sperm-Specific Activator of CFTR, Are Associated with Human Asthenozoospermia. The American Journal of Human Genetics. 2013 May;92(5):760–6. doi: 10.1016/j.ajhg.2013.03.016.
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date	2013-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/23582645 https://pubmed.ncbi.nlm.nih.gov/PMC3644633 https://doi.org/10.1016/j.ajhg.2013.03.016
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Missense Mutations in SLC26A8, Encoding a Sperm-Specific Activator of CFTR, Are Associated with Human Asthenozoospermia
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