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SIX1

MIM.601205 14q23

Thursday 22 March 2007

Pathology

- germline mutations in

  • branchiootorenal syndrome (MIM.113650) (branchiootic syndrome type 3 or BOS3) (MIM.608389)
  • autosomal dominant deafness type 23 (DFNA23) (MIM.605192)

See also

- SIXs