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Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases.

AUTHOR(S): Audo I, Bujakowska KM, Leveillard T, Mohand-Said S, Lancelot ME, Germain A, Antonio A, Michiels C, Saraiva JP, Letexier M, Sahel JA et al.

TITLE: Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases. Orphanet J Rare Dis 2012, Jan 25, 7:8.

SOURCE

Copyright © 2012 Audo et al; licensee BioMed Central Ltd.