Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) syndrome associated with mutations inKIF11-Reference-Cited by-同舟云学术

Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) syndrome associated with mutations inKIF11

Published:2015-05-21 Issue:1 Volume:94 Page:92-98
ISSN:1755-375X
Container-title:Acta Ophthalmologica
language:en
Short-container-title:Acta Ophthalmol

Author:

Balikova Irina¹²,Robson Anthony G.¹³,Holder Graham E.¹³,Ostergaard Pia⁴,Mansour Sahar⁵,Moore Anthony T.¹³

Affiliation:

1. Moorfields Eye Hospital; London UK

2. Free University of Brussels; Brussels Belgium

3. UCL Institute of Ophthalmology; London UK

4. Cardiovascular & Cell Sciences Research Institute; St George's University of London; London UK

5. SW Thames Regional Genetics Service; St George's Healthcare NHS Trust; London UK

Funder

Fight for Sight

Foundation Fighting Blindness

National Institute for Health Research

British Heart Foundation

Publisher

Wiley

Subject

Ophthalmology,General Medicine

Reference23 articles.

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3. ISCEV standard for clinical pattern electroretinography (PERG): 2012 update;Bach;Doc Ophthalmol,2013

4. Phosphorylation by p34cdc2 regulates spindle association of human Eg5, a kinesin-related motor essential for bipolar spindle formation in vivo;Blangy;Cell,1995

5. Autosomal dominant microcephaly-lymphoedema-chorioretinal dysplasia syndrome;Casteels;Br J Ophthalmol,2001

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