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Chromosome 11


USH1C

Usher syndrome 1C (autosomal recessive, severe)

  • Location: Chromosome 11, NC_000011.10 (17493895..17544416, complement)
  • PDB Entries
  • Diseases: Usher syndrome Retinitis pigmentosa Nonsyndromic deafnesss
  • Jensen Lab Disease Associations
  • Publications List from GeneCards.org
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