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Browsing by Author Estrada-Cuzcano, A.
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| Full Text | Issue Date | Title | Author(s) | | 2011 | IQCB1 mutations in patients with leber congenital amaurosis | Estrada-Cuzcano, A.; Koenekoop, R.K.; Coppieters, F.; Kohl, S.; Lopez, I., et al |
| 2010 | Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy. | Otto, E.A.; Hurd, T.W.; Airik, R.; Chaki, M.; Zhou, W., et al |
| 2009 | A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies. | Khanna, H.; Davis, E.E.; Murga-Zamalloa, C.A.; Estrada-Cuzcano, A.; Lopez, I., et al |
Showing results 1 to 3 of 3
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