Comment: Novel mutations in the OPN1LW and NR2R3 genes in a patient with blue cone monochromacy. (2nd November 2019)

Record Type:: Journal Article
Title:: Comment: Novel mutations in the OPN1LW and NR2R3 genes in a patient with blue cone monochromacy. (2nd November 2019)
Main Title:: Comment: Novel mutations in the OPN1LW and NR2R3 genes in a patient with blue cone monochromacy
Authors:: Escher, Pascal
Abstract:
Is Part Of:: Ophthalmic genetics. Volume 40:Number 6(2019)
Journal:: Ophthalmic genetics
Issue:: Volume 40:Number 6(2019)
Issue Display:: Volume 40, Issue 6 (2019)
Year:: 2019
Volume:: 40
Issue:: 6
Issue Sort Value:: 2019-0040-0006-0000
Page Start:: 591
Page End:: 591
Publication Date:: 2019-11-02
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:: 10.1080/13816810.2019.1573908 ↗
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
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Ingest File:: 12740.xml