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Bi-allelic mutations in M1AP are a frequent cause of meiotic arrest and severely impaired spermatogenesis leading to male infertility

Lookup NU author(s): James Heald, Kevin McEleny, Dr Miguel Garcia Dos Santos XavierORCiD, Professor Joris VeltmanORCiD

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This is the authors' accepted manuscript of an article that has been published in its final definitive form by Cell Press, 2020.

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Author(s): Wyrwoll MJ, Temel SG, Nagirnaja L, Oud MS, Lopes AM, van der Heijden GW, Heald JS, Rotte N, Wistuba J, Wöste M, Ledig S, Krenz H, Smits RM, Carvalho F, Gonçalves J, Fietz D, Türkgenç B, Ergören MC, Cetinkaya M, Basar M, Kahraman S, McEleny K, Xavier MJ, Turner H, Pilatz A, Röpke A, Dugas M, Kliesch S, Neuhaus N, Aston KI, Conrad DF, Veltman JA, Friedrich C, Tüttelmann F

Publication type: Article

Publication status: Published

Journal: American Journal of Human Genetics

Year: 2020

Volume: 107

Issue: 2

Pages: 342-351

Print publication date: 06/08/2020

Online publication date: 15/07/2020

Acceptance date: 12/06/2020

Date deposited: 24/06/2020

ISSN (print): 0002-9297

ISSN (electronic): 1537-6605

Publisher: Cell Press

URL: https://doi.org/10.1016/j.ajhg.2020.06.010

DOI: 10.1016/j.ajhg.2020.06.010

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