Published in
Wiley, Acta Ophthalmologica, 3(90), p. e192-e197, 2011
DOI: 10.1111/j.1755-3768.2011.02267.x
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A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene.
Journal article published in 2011 by
Pi Sergouniotis,
Ag Robson,
Zheng Li 
,
Sophie Devery,
Ge Holder,
At Moore,
Ar Webster
,
Sophie Devery,
Ge Holder,
At Moore,
Ar Webster
This paper is made freely available by the publisher.
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Abstract
To describe the clinical phenotype and the molecular pathology in a group of patients with congenital stationary night blindness due to mutations in GRM6, a gene encoding the ON bipolar metabotropic glutamate receptor 6 (mGluR6).