Kotan, L. D., Ternier, G., Cakir, A. D., Emeksiz, H. C., Turan, i., Delpouve, G., . . . Kemal Topaloglu, A. (2021). Loss-of-Function Mutations in SEMA3F and gePLXNA3 Encoding Semaphorin-3F and its Receptor Plexin-A3 Respectively Cause Idiopathic Hypogonadotropic Hypogonadism. Genet Med.
Citação norma ChicagoKotan, Leman Damla, et al. "Loss-of-Function Mutations in SEMA3F and GePLXNA3 Encoding Semaphorin-3F and Its Receptor Plexin-A3 Respectively Cause Idiopathic Hypogonadotropic Hypogonadism." Genet Med 2021.
MLA CitationKotan, Leman Damla, et al. "Loss-of-Function Mutations in SEMA3F and GePLXNA3 Encoding Semaphorin-3F and Its Receptor Plexin-A3 Respectively Cause Idiopathic Hypogonadotropic Hypogonadism." Genet Med 2021.
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