Heterozygous GGC repeat expansion of NOTCH2NLC in a patient with neuronal intranuclear inclusion disease and progressive retinal dystrophy. (2nd January 2020)

Record Type:
Journal Article
Title:
Heterozygous GGC repeat expansion of NOTCH2NLC in a patient with neuronal intranuclear inclusion disease and progressive retinal dystrophy. (2nd January 2020)
Main Title:
Heterozygous GGC repeat expansion of NOTCH2NLC in a patient with neuronal intranuclear inclusion disease and progressive retinal dystrophy
Authors:
Hayashi, Takaaki
Katagiri, Satoshi
Mizobuchi, Kei
Yoshitake, Kazutoshi
Kameya, Shuhei
Matsuura, Tomokazu
Iwata, Takeshi
Nakano, Tadashi
Abstract:
Is Part Of:
Ophthalmic genetics. Volume 41:Number 1(2020)
Journal:
Ophthalmic genetics
Issue:
Volume 41:Number 1(2020)
Issue Display:
Volume 41, Issue 1 (2020)
Year:
2020
Volume:
41
Issue:
1
Issue Sort Value:
2020-0041-0001-0000
Page Start:
93
Page End:
95
Publication Date:
2020-01-02
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:
10.1080/13816810.2020.1723119 ↗
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:
22494.xml