Comprehensive sequence analysis of nine Usher syndrome genes in the UK National Collaborative Usher Study

Polona Le Quesne Stabej; Zubin Saihan; Nell Rangesh; Heather B Steele-Stallard; John Ambrose; Alison Coffey; Jenny Emmerson; Elene Haralambous; Yasmin Hughes; Karen P Steel; Linda M Luxon; Andrew R Webster; Maria Bitner-Glindzicz

doi:10.1136/jmedgenet-2011-100468

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Genotype-phenotype correlations

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Comprehensive sequence analysis of nine Usher syndrome genes in the UK National Collaborative Usher Study

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Polona Le Quesne Stabej Clinical and Molecular Genetics, Institute of Child Health, UCL, London, UK PubMed articles Google scholar articles
Zubin Saihan Institute of Ophthalmology, UCL, London, UK Moorfields Eye Hospital, London, UK PubMed articles Google scholar articles
Nell Rangesh Audiovestibualar Medicine, Institute of Child Health, UCL, London, UK PubMed articles Google scholar articles
Heather B Steele-Stallard Clinical and Molecular Genetics, Institute of Child Health, UCL, London, UK PubMed articles Google scholar articles
John Ambrose Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK PubMed articles Google scholar articles
Alison Coffey Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK PubMed articles Google scholar articles
Jenny Emmerson Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK PubMed articles Google scholar articles
Elene Haralambous Clinical and Molecular Genetics, Institute of Child Health, UCL, London, UK PubMed articles Google scholar articles
Yasmin Hughes Clinical and Molecular Genetics, Institute of Child Health, UCL, London, UK PubMed articles Google scholar articles
Karen P Steel Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK PubMed articles Google scholar articles
Linda M Luxon Audiovestibualar Medicine, Institute of Child Health, UCL, London, UK UCL Ear Institute, London, UK PubMed articles Google scholar articles
Andrew R Webster Institute of Ophthalmology, UCL, London, UK Moorfields Eye Hospital, London, UK PubMed articles Google scholar articles
Maria Bitner-Glindzicz Clinical and Molecular Genetics, Institute of Child Health, UCL, London, UK UCL Ear Institute, London, UK PubMed articles Google scholar articles

Correspondence to Dr Maria Bitner-Glindzicz, Clinical and Molecular Genetics Unit, Institute of Child Health, UCL, 30 Guilford Street, London WC1N 1EH, UK; mbitnerg{at}ich.ucl.ac.uk

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Citation

Le Quesne Stabej P, Saihan Z, Rangesh N, et al

Comprehensive sequence analysis of nine Usher syndrome genes in the UK National Collaborative Usher Study

Journal of Medical Genetics 2012;49:27-36.

Publication history

Received August 31, 2011
Revised October 13, 2011
Accepted October 15, 2011
First published December 1, 2011.

Online issue publication

December 13, 2011

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© 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/3.0/ and http://creativecommons.org/licenses/by-nc/3.0/legalcode

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