Missense Mutations in SLC26A8, Encoding a Sperm-Specific Activator of CFTR, Are Associated with Human Asthenozoospermia-Reference-Cited by-同舟云学术

Missense Mutations in SLC26A8, Encoding a Sperm-Specific Activator of CFTR, Are Associated with Human Asthenozoospermia

Published:2013-05 Issue:5 Volume:92 Page:760-766
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Dirami Thassadite,Rode Baptiste,Jollivet Mathilde,Da Silva Nathalie,Escalier Denise,Gaitch Natacha,Norez Caroline,Tuffery Pierre,Wolf Jean-Philippe,Becq Frédéric,Ray Pierre F.,Dulioust Emmanuel,Gacon Gérard,Bienvenu Thierry,Touré Aminata

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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