Cockayne syndrome type A: novel mutations in eight typical patients (2006)
Source: Journal of human genetics. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, GENÓTIPOS, FENÓTIPOS, DOENÇAS NEURODEGENERATIVAS
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BERTOLA, Debora R. et al. Cockayne syndrome type A: novel mutations in eight typical patients. Journal of human genetics, v. 51, n. 8, p. 701-705, 2006Tradução . . Disponível em: https://doi.org/10.1007/s10038-006-0011-7. Acesso em: 06 jun. 2024.APA
Bertola, D. R., Cao, H., Albano, L. M. J., Kok, F., Marques-Dias, M. J., Kim, C. A., & Hegele, R. A. (2006). Cockayne syndrome type A: novel mutations in eight typical patients. Journal of human genetics, 51( 8), 701-705. doi:10.1007/s10038-006-0011-7NLM
Bertola DR, Cao H, Albano LMJ, Kok F, Marques-Dias MJ, Kim CA, Hegele RA. Cockayne syndrome type A: novel mutations in eight typical patients [Internet]. Journal of human genetics. 2006 ;51( 8): 701-705.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1007/s10038-006-0011-7Vancouver
Bertola DR, Cao H, Albano LMJ, Kok F, Marques-Dias MJ, Kim CA, Hegele RA. Cockayne syndrome type A: novel mutations in eight typical patients [Internet]. Journal of human genetics. 2006 ;51( 8): 701-705.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1007/s10038-006-0011-7
