Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram. (Q34462879)
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- Mutations inGRM6Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram. |
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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