Cita APA

AlFadhli, S., Abdelmoaty, S., Al-Hajeri, A., Behbehani, A., & Alkuraya, F. (2012). Novel crystallin gamma B mutations in a Kuwaiti family with autosomal dominant congenital cataracts reveal genetic and clinical heterogeneity. Molecular Vision.

Citación estilo Chicago

AlFadhli, Suad, Sidky Abdelmoaty, Amal Al-Hajeri, Abdulmutalib Behbehani, y Fowzan Alkuraya. Novel Crystallin Gamma B Mutations in a Kuwaiti Family With Autosomal Dominant Congenital Cataracts Reveal Genetic and Clinical Heterogeneity. Molecular Vision, 2012.

Cita MLA

AlFadhli, Suad, et al. Novel Crystallin Gamma B Mutations in a Kuwaiti Family With Autosomal Dominant Congenital Cataracts Reveal Genetic and Clinical Heterogeneity. Molecular Vision, 2012.