Chamberlin, Adam; Huether, Robert; Machado, Aline Z; Groden, Michael; Liu, Hsiao-Mei; Upadhyay, Kinnari; Vivian, O; Gomes, Nathalia L; Lerario, Antonio M; Mendonça, Berenice Bilharinho de 
Fonte: Human molecular genetics. Unidade: FM
Assuntos: TRANSTORNOS DO DESENVOLVIMENTO SEXUAL, PROTEÍNAS QUINASES, MUTAÇÃO GENÉTICA, GENÉTICA MOLECULAR
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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: 03 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. 03 ] 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. 03 ] Available from: https://doi.org/10.1093/hmg/ddz002
