A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataract-Reference-Cited by-同舟云学术

A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataract

Published:2017-10-17 Issue:2 Volume:39 Page:236-241
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Berry Vanita¹,Pontikos Nikolas¹²^ORCID,Albarca-Aguilera Monica³,Plagnol Vincent²,Massouras Andreas³,Prescott DeQuincy¹,Moore Anthony T.⁴,Arno Gavin¹,Cheetham Michael E.¹,Michaelides Michel¹⁵

Affiliation:

1. Genetics, UCL Institute of Ophthalmology, London, UK

2. Genetics, UCL Genetics Institute, London, UK

3. Sephator, Geneva, Switzerland

4. Ophthalmology, San Francisco, UCSF, USA

5. Ophthalmology, Moorfields Eye Hospital, London, UK

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2017.1381977

Reference27 articles.

1. Molecular genetic basis of inherited cataract and associated phenotypes

2. Contents, Vol. 210, No. 1, 1996

3. Clinical and experimental advances in congenital and paediatric cataracts

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