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Search results 1 to 1 out of 1 for Rd3

Category restricted to ProteinDomain (x)

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Category: ProteinDomain
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Type Details Score
Protein Domain
IPR028092 | RD3
Type: Family
Description: In humans, Retinal degeneration protein 3 (RD3) is found preferentially expressed in the retina []. Mutations in RD3 causes Leber Congenital Amaurosis type 12 ,which is a severe dystrophy of the retina, typically becoming evident in the first years of life [].
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