Novel homozygous mutation in the SPATA7 gene causes autosomal recessive retinal degeneration in a consanguineous

Authors

Feldhaus B1, Kohl S2, Hörtnagel K3, Weisschuh N2, Zobor D1.
  1. a Institute for Ophthalmic Research, Centre for Ophthalmology , University of Tübingen , Tübingen , Germany.
  2. b Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology , University of Tübingen , Tübingen , Germany.
  3. c Praxis für Humangenetik Tübingen & CeGaT GmbH , Tübingen , Germany.