(Q27674860)

English

Leber congenital amaurosis 15

A Leber congenital amaurosis that has material basis in mutation in the TULP1 gene on chromosome 6p21.3.

  • LCA15
  • LEBER CONGENITAL AMAUROSIS 15; LCA15
  • LEBER CONGENITAL AMAUROSIS 15
  • Leber Congenital Amaurosis type 15
  • Retinitis Pigmentosa, Juvenile, Tulp1-Related

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