(Q27677680)

English

Leber congenital amaurosis 11

A Leber congenital amaurosis that has material basis in mutation n the IMPDH1 gene on chromosome 7q31.3-q32.

  • LCA11
  • LEBER CONGENITAL AMAUROSIS 11
  • LEBER CONGENITAL AMAUROSIS 11; LCA11
  • Leber congenital amaurosis type 11
  • Amaurosis congenita of Leber, type 11

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