RICHARD GIBBS to Leber Congenital Amaurosis
This is a "connection" page, showing publications RICHARD GIBBS has written about Leber Congenital Amaurosis.
Connection Strength
0.190
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Exome capture sequencing identifies a novel mutation in BBS4. Mol Vis. 2011; 17:3529-40.
Score: 0.096
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Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis. Hum Mutat. 2011 Dec; 32(12):1450-9.
Score: 0.094