Source: American journal of human genetics. Unidade: FM
Subjects: OSSO E OSSOS, LINHAGEM CELULAR, OSTEOGÊNESE, TRANSDUÇÃO DE SINAL CELULAR, CAMUNDONGOS
ABNT
LIN, Yuh-Charn et al. SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling. American journal of human genetics, v. 108, n. 1, p. 115-133, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2020.11.015. Acesso em: 17 out. 2024.APA
Lin, Y. -C., Niceta, M., Muto, V., Vona, B., Pagnamenta, A. T., Maroofian, R., et al. (2021). SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling. American journal of human genetics, 108( 1), 115-133. doi:10.1016/j.ajhg.2020.11.015NLM
Lin Y-C, Niceta M, Muto V, Vona B, Pagnamenta AT, Maroofian R, Beetz C, Duyvenvoorde H van, Dentici ML, Jorge AA de L. SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling [Internet]. American journal of human genetics. 2021 ; 108( 1): 115-133.[citado 2024 out. 17 ] Available from: https://doi.org/10.1016/j.ajhg.2020.11.015Vancouver
Lin Y-C, Niceta M, Muto V, Vona B, Pagnamenta AT, Maroofian R, Beetz C, Duyvenvoorde H van, Dentici ML, Jorge AA de L. SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling [Internet]. American journal of human genetics. 2021 ; 108( 1): 115-133.[citado 2024 out. 17 ] Available from: https://doi.org/10.1016/j.ajhg.2020.11.015