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Posts tagged CRISPR/Cas9

Natural History Study Launches for LCA Caused by Specific Mutation in CEP290

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The Massachusetts Eye and Ear Infirmary (MEEI) and other centers in the US and Europe are conducting a natural history study for people with Leber congenital amaurosis 10 (LCA10) caused by a mutation referred to as “intron 26 c.2991+1655A>G” in the CEP290 gene.
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