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

February 01, 2018

Feldhaus B1, Kohl S2, Hörtnagel K3, Weisschuh N2, Zobor D1.

Abstract

No abstract available

  1. Institute for Ophthalmic Research, Centre for Ophthalmology , University of Tübingen , Tübingen , Germany.
  2. Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology , University of Tübingen , Tübingen , Germany.
  3. Praxis für Humangenetik Tübingen & CeGaT GmbH , Tübingen , Germany.