Expression ofPRPF31mRNA in Patients with Autosomal Dominant Retinitis Pigmentosa: A Molecular Clue for Incomplete Penetrance?-Reference-Cited by-同舟云学术

Expression ofPRPF31mRNA in Patients with Autosomal Dominant Retinitis Pigmentosa: A Molecular Clue for Incomplete Penetrance?

Published:2003-10-01 Issue:10 Volume:44 Page:4204
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Vithana Eranga N.¹,Abu-Safieh Leen¹,Pelosini Lucia²,Winchester Elizabeth²,Hornan Dan¹,Bird Alan C.²,Hunt David M.¹,Bustin Stephen A.³,Bhattacharya Shomi S.¹

Affiliation:

1. From the Division of Molecular Genetics, Institute of Ophthalmology, University College London, London, United Kingdom; the

2. Moorfields Eye Hospital, London, United Kingdom; and the

3. Academic Department of Surgery, St. Bartholomews and the Queen Mary’s School of Medicine and Dentistry, University of London, London, United Kingdom.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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