Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice

Author:

Coutton Charles,Martinez Guillaume,Kherraf Zine-Eddine,Amiri-Yekta Amir,Boguenet Magalie,Saut Antoine,He Xiaojin,Zhang Feng,Cristou-Kent Marie,Escoffier Jessica,Bidart Marie,Satre Véronique,Conne Béatrice,Fourati Ben Mustapha Selima,Halouani Lazhar,Marrakchi Ouafi,Makni Mounir,Latrous Habib,Kharouf Mahmoud,Pernet-Gallay Karin,Bonhivers Mélanie,Hennebicq Sylviane,Rives Nathalie,Dulioust Emmanuel,Touré Aminata,Gourabi Hamid,Cao Yunxia,Zouari Raoudha,Hosseini Seyedeh Hanieh,Nef Serge,Thierry-Mieg Nicolas,Arnoult Christophe,Ray Pierre F.

Funder

French Agence Nationale pour la Recherche

Direction Générale de l’Offre de Soin

Fondation Maladies Rares

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference36 articles.

1. Unraveling transcriptome dynamics in human spermatogenesis;Jan;Development,2017

2. Disorders of spermatogenesis: Perspectives for novel genetic diagnostics after 20 years of unchanged routine;Tüttelmann;Med. Genetik,2018

3. Genetics of male infertility;Krausz;Nat. Rev. Urol.,2018

4. Teratozoospermia: spotlight on the main genetic actors in the human;Coutton;Hum. Reprod. Update,2015

5. Genetic abnormalities leading to qualitative defects of sperm morphology or function;Ray;Clin. Genet.,2017

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