DOI: 10.1055/s-00000072

Seminars in Reproductive Medicine

References

Faridi R, Rehman AU, Morell RJ. , et al.
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

Clin Genet 2017;
91 (02) 328-332

Download Bibliographical Data

Access:
Access: