Source: Human molecular genetics. Unidade: FM
Subjects: TRANSTORNOS DO DESENVOLVIMENTO SEXUAL, PROTEÍNAS QUINASES, MUTAÇÃO GENÉTICA, GENÉTICA MOLECULAR
ABNT
CHAMBERLIN, Adam et al. Mutations in MAP3K1 that cause 46,XY disorders of sex development disrupt distinct structural domains in the protein. Human molecular genetics, v. 28, n. 10, p. 1620-1628, 2019Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddz002. Acesso em: 14 out. 2024.APA
Chamberlin, A., Huether, R., Machado, A. Z., Groden, M., Liu, H. -M., Upadhyay, K., et al. (2019). Mutations in MAP3K1 that cause 46,XY disorders of sex development disrupt distinct structural domains in the protein. Human molecular genetics, 28( 10), 1620-1628. doi:10.1093/hmg/ddz002NLM
Chamberlin A, Huether R, Machado AZ, Groden M, Liu H-M, Upadhyay K, Vivian O, Gomes NL, Lerario AM, Mendonça BB de. Mutations in MAP3K1 that cause 46,XY disorders of sex development disrupt distinct structural domains in the protein [Internet]. Human molecular genetics. 2019 ; 28( 10): 1620-1628.[citado 2024 out. 14 ] Available from: https://doi.org/10.1093/hmg/ddz002Vancouver
Chamberlin A, Huether R, Machado AZ, Groden M, Liu H-M, Upadhyay K, Vivian O, Gomes NL, Lerario AM, Mendonça BB de. Mutations in MAP3K1 that cause 46,XY disorders of sex development disrupt distinct structural domains in the protein [Internet]. Human molecular genetics. 2019 ; 28( 10): 1620-1628.[citado 2024 out. 14 ] Available from: https://doi.org/10.1093/hmg/ddz002