Mutations in PCYT1A cause spondylometaphyseal dysplasia with cone-rod dystrophy (2014)
Yamamoto, Guilherme L.; Baratela, Wagner A. R.; Almeida, Tatiana F.; Lazar, Monize; Afonso, Clara L.; Oyamada, Maria K.; Suzuki, Lisa; Oliveira, Luiz A. N.; Ramos, Ester Silveira; Kim, Chong Ae; Passos-Bueno, Maria Rita 
; Bertola, Débora Romeo
Source: American Journal of Human Genetics. Unidades: FMRP, FM, IB
Subjects: OFTALMOLOGIA (MÉTODOS), DOENÇAS RETINIANAS (GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
YAMAMOTO, Guilherme L. et al. Mutations in PCYT1A cause spondylometaphyseal dysplasia with cone-rod dystrophy. American Journal of Human Genetics, v. 94, n. 1, p. 113-119, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2013.11.022. Acesso em: 04 nov. 2024.APA
Yamamoto, G. L., Baratela, W. A. R., Almeida, T. F., Lazar, M., Afonso, C. L., Oyamada, M. K., et al. (2014). Mutations in PCYT1A cause spondylometaphyseal dysplasia with cone-rod dystrophy. American Journal of Human Genetics, 94( 1), 113-119. doi:10.1016/j.ajhg.2013.11.022NLM
Yamamoto GL, Baratela WAR, Almeida TF, Lazar M, Afonso CL, Oyamada MK, Suzuki L, Oliveira LAN, Ramos ES, Kim CA, Passos-Bueno MR, Bertola DR. Mutations in PCYT1A cause spondylometaphyseal dysplasia with cone-rod dystrophy [Internet]. American Journal of Human Genetics. 2014 ; 94( 1): 113-119.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.ajhg.2013.11.022Vancouver
Yamamoto GL, Baratela WAR, Almeida TF, Lazar M, Afonso CL, Oyamada MK, Suzuki L, Oliveira LAN, Ramos ES, Kim CA, Passos-Bueno MR, Bertola DR. Mutations in PCYT1A cause spondylometaphyseal dysplasia with cone-rod dystrophy [Internet]. American Journal of Human Genetics. 2014 ; 94( 1): 113-119.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.ajhg.2013.11.022
