Long-term follow-up of a patient with JAG1-associated retinopathy-Reference-Cited by-同舟云学术

Long-term follow-up of a patient with JAG1-associated retinopathy

Published:2021-04-20 Issue:2 Volume:143 Page:237-247
ISSN:0012-4486
Container-title:Documenta Ophthalmologica
language:en
Short-container-title:Doc Ophthalmol

Author:

Cheema Muhammad R.,Stone Lydia G.,Sellar Peter W.,Quinn Stephanie,Clark Stephen C.,Martin Richard J.,O’Brien Jill M.,Warriner Clare,Browning Andrew C.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Physiology (medical),Sensory Systems,Ophthalmology

Link

https://link.springer.com/content/pdf/10.1007/s10633-021-09836-w.pdf

Reference38 articles.

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2. Oda T, Elkahloun AG, Pike BL et al (1997) Mutations in the human Jagged1 gene are responsible for Alagille syndrome. Nat Genet 16:235–242

3. Zhang L, Zhang X, Xu H, Huang L, Zhang S, Liu W et al (2020) Exome sequencing revealed Notch ligand JAG1 as a novel candidate gene for familial exudative vitreoretinopathy. Genet Med 22:77–84

4. Danks DM, Campbell PE, Jack I, Rogers J, Smith AL (1977) Studies of the aetiology of neonatal hepatitis and biliary atresia. Arch Dis Child 52:360–367

5. Alagille D, Estrada A, Hadchouel M, Gautier M (1987) Odie`vre M, Dommergues JP: syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases. J Pediat 110:195–200

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