Identification of a novel GRM6 mutation in a previously described consanguineous family with complete congenital stationary night blindness. (4th March 2019)

Record Type:
Journal Article
Title:
Identification of a novel GRM6 mutation in a previously described consanguineous family with complete congenital stationary night blindness. (4th March 2019)
Main Title:
Identification of a novel GRM6 mutation in a previously described consanguineous family with complete congenital stationary night blindness
Authors:
Tourville, Aurore
Michiels, Christelle
Condroyer, Christel
Meunier, Audrey
Cordonnier, Monique
Sahel, José-Alain
Audo, Isabelle
Abramowicz, Marc
Zeitz, Christina
Abstract:
Is Part Of:
Ophthalmic genetics. Volume 40:Number 2(2019)
Journal:
Ophthalmic genetics
Issue:
Volume 40:Number 2(2019)
Issue Display:
Volume 40, Issue 2 (2019)
Year:
2019
Volume:
40
Issue:
2
Issue Sort Value:
2019-0040-0002-0000
Page Start:
182
Page End:
184
Publication Date:
2019-03-04
Subjects:
Eye -- Diseases -- Genetic aspects -- Periodicals
Eye Diseases -- genetics -- Periodicals
Eye Diseases -- in infancy & childhood -- Periodicals
617.7
Journal URLs:
http://informahealthcare.com/loi/opg ↗
http://informahealthcare.com ↗
http://www.tandf.co.uk/journals/titles/13816810.asp ↗
DOI:
10.1080/13816810.2019.1605389 ↗
Languages:
English
ISSNs:
1381-6810
Deposit Type:
Legaldeposit
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:
British Library DSC - 6270.893000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:
10103.xml