(Q27677618)

English

Leber congenital amaurosis 12

Leber congenital amaurosis that has material basis in mutation in the RD3 gene on chromosome 1q32

  • LCA12
  • Leber Congenital Amaurosis type 12
  • LEBER CONGENITAL AMAUROSIS 12
  • LEBER CONGENITAL AMAUROSIS 12; LCA12
  • Amaurosis congenita of Leber, type 12
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