Source: American Journal of Human Genetics. Unidades: IB, FM
Subjects: DEGENERAÇÃO RETINIANA, DOENÇAS RETINIANAS, CEGUEIRA
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SUZUKI, Oscar T. et al. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics, v. 71, p. 1320-1329, 2002Tradução . . Acesso em: 03 out. 2024.APA
Suzuki, O. T., Sertié, A. L., Der Kaloustian, V. M., Kok, F., Carpenter, M., Murray, J., et al. (2002). Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics, 71, 1320-1329.NLM
Suzuki OT, Sertié AL, Der Kaloustian VM, Kok F, Carpenter M, Murray J, Czeizel AE, Kliemann SE, Rosemberg S, Monteiro M, Olsen BR, Passos-Bueno MR. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics. 2002 ; 71 1320-1329.[citado 2024 out. 03 ]Vancouver
Suzuki OT, Sertié AL, Der Kaloustian VM, Kok F, Carpenter M, Murray J, Czeizel AE, Kliemann SE, Rosemberg S, Monteiro M, Olsen BR, Passos-Bueno MR. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics. 2002 ; 71 1320-1329.[citado 2024 out. 03 ]