TACR3 mutations disrupt NK3R function through distinct mechanisms in GnRH-deficient patients (2014)
Source: The FASEB journal. Unidade: FM
Subjects: SEQUENCIAMENTO GENÉTICO, MUTAÇÃO GENÉTICA (COMPLICAÇÕES), HIPOGONADISMO
ABNT
NOEL, Sekoni D. et al. TACR3 mutations disrupt NK3R function through distinct mechanisms in GnRH-deficient patients. The FASEB journal, v. 28, n. 4, p. 1924-1937, 2014Tradução . . Disponível em: https://doi.org/10.1096/fj.13-240630. Acesso em: 05 out. 2024.APA
Noel, S. D., Abreu, A. P., Xu, S., Muyide, T., Gianetti, E., Tusset, C., et al. (2014). TACR3 mutations disrupt NK3R function through distinct mechanisms in GnRH-deficient patients. The FASEB journal, 28( 4), 1924-1937. doi:10.1096/fj.13-240630NLM
Noel SD, Abreu AP, Xu S, Muyide T, Gianetti E, Tusset C, Carroll J, Latronico AC, Seminara SB, Carroll RS, Kaiser UB. TACR3 mutations disrupt NK3R function through distinct mechanisms in GnRH-deficient patients [Internet]. The FASEB journal. 2014 ; 28( 4): 1924-1937.[citado 2024 out. 05 ] Available from: https://doi.org/10.1096/fj.13-240630Vancouver
Noel SD, Abreu AP, Xu S, Muyide T, Gianetti E, Tusset C, Carroll J, Latronico AC, Seminara SB, Carroll RS, Kaiser UB. TACR3 mutations disrupt NK3R function through distinct mechanisms in GnRH-deficient patients [Internet]. The FASEB journal. 2014 ; 28( 4): 1924-1937.[citado 2024 out. 05 ] Available from: https://doi.org/10.1096/fj.13-240630