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
Publisher: ELSEVIER SCIENCE INC
: 2013
: Fertility and Sterility
: FERTILITY AND STERILITY
: FERTIL STERIL
: 3
: 99
: 3
: 815
: 818
: 4
: 0015-0282
DOI: https://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.)