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APA Citation
Caburet, S., Fruchter, R. B., Legois, B., Fellous, M., Shalev, S., & Veitia, R. A. (2017). a homozygous mutation of GNRHR in a familial case diagnosed with polycystic ovary syndrome. European journal of endocrinology, 176(5), K9–K14. http://access.bl.uk/ark:/81055/vdc_100044984936.0x000012