(Q34462879)
English
Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.
scientific article
- Mutations inGRM6Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram
Statements
Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram (English)
Maria van Genderen
John Neidhardt
Ulrich F O Luhmann
Frank Hoeben
Ursula Forster
Katharina Wycisk
Carel B Hoyng
Frans Riemslag
Françoise Meire
Frans P M Cremers
Wolfgang Berger
1 November 2005