PROKR2 mutations in autosomal recessive Kallmann syndrome




Tommiska J, Toppari J, Vaaralahti K, Kansakoski J, Laitinen EM, Noisa P, Kinnala A, Niinikoski H, Raivio T

PublisherELSEVIER SCIENCE INC

2013

Fertility and Sterility

FERTILITY AND STERILITY

FERTIL STERIL

3

99

3

815

818

4

0015-0282

DOIhttps://doi.org/10.1016/j.fertnstert.2012.11.003



Conclusion(s): These findings are consistent with recessive mode of inheritance. PROKR2 signaling does not directly affect Sertoli cell function. (Fertil Steril (R) 2013;99:815-8. (C) 2013 by American Society for Reproductive Medicine.)



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