Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | Date | No Grouping
Jump to: 2015
Number of items: 2.

2015

Coppieters, Frauke, Bauwens, Miriam, Karlstetter, Marcus, Vleminckx, Kris, Van der Eecken, Morgane, Langmann, Thomas, Leroy, Bart Peter, Meire, Francoise and De Baere, Elfride ORCID: 0000-0002-5609-6895 (2015). Mutation of RCBTB1 in a severe syndromic retinal ciliopathy. Invest. Ophthalmol. Vis. Sci., 56 (7). ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC. ISSN 1552-5783

Van Cauwenbergh, Caroline, Vleminckx, Kris, Coppieters, Frauke, Karlstetter, Marcus, Langmann, Thomas, Manes, Gael, Hamel, Christian P., Leroy, Bart Peter and De Baere, Elfride ORCID: 0000-0002-5609-6895 (2015). SF3B2, a novel candidate gene for autosomal dominant retinitis pigmentosa, encodes a component of the U2 small nuclear ribonucleoprotein. Invest. Ophthalmol. Vis. Sci., 56 (7). ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC. ISSN 1552-5783

This list was generated on Thu Apr 25 10:59:04 2024 CEST.