Review and update on the molecular basis of Leber congenital amaurosis

doi:10.12998/wjcc.v3.i2.112

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Feb 16, 2015 (publication date) through Nov 26, 2024

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World Journal of Clinical Cases

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2307-8960

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

Review

World J Clin Cases. Feb 16, 2015; 3(2): 112-124
Published online Feb 16, 2015. doi: 10.12998/wjcc.v3.i2.112

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Figure 1 Patient´s fundus with RPE65 mutations.

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Figure 2 Patient´s fundus with CRB1 mutations.

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Figure 3 Patient´s fundus with RDH12 mutations.

Citation: Chacon-Camacho OF, Zenteno JC. Review and update on the molecular basis of Leber congenital amaurosis. World J Clin Cases 2015; 3(2): 112-124
URL: https://www.wjgnet.com/2307-8960/full/v3/i2/112.htm
DOI: https://dx.doi.org/10.12998/wjcc.v3.i2.112