Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility

Author:

Wyrwoll Margot J.,Temel Şehime G.,Nagirnaja Liina,Oud Manon S.,Lopes Alexandra M.,van der Heijden Godfried W.,Heald James S.,Rotte Nadja,Wistuba Joachim,Wöste Marius,Ledig Susanne,Krenz Henrike,Smits Roos M.,Carvalho Filipa,Gonçalves João,Fietz Daniela,Türkgenç Burcu,Ergören Mahmut C.,Çetinkaya Murat,Başar Murad,Kahraman Semra,McEleny Kevin,Xavier Miguel J.,Turner Helen,Pilatz Adrian,Röpke Albrecht,Dugas Martin,Kliesch Sabine,Neuhaus Nina,Aston Kenneth I.,Conrad Donald F.,Veltman Joris A.,Friedrich Corinna,Tüttelmann Frank

Funder

National Institutes of Health

Deutsche Forschungsgemeinschaft

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference25 articles.

1. Regional differences in waiting time to pregnancy: pregnancy-based surveys from Denmark, France, Germany, Italy and Sweden. The European Infertility and Subfecundity Study Group;Juul;Hum. Reprod.,1999

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

3. WHO laboratory manual for the examination and processing of human semen,2010

4. Role of genetics in azoospermia;Lee;Urology,2011

5. X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men;Yatsenko;N. Engl. J. Med.,2015

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