Protein Domain : Retinal degeneration protein 3 IPR028092

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 [].
Short Name  RD3

0 Child Features

0 Gene Families

0 Genes

0 Ontology Annotations

0 Parent Features

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