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

✍ Scribed by Isabelle Audo, Kinga M Bujakowska, Thierry Léveillard, Saddek Mohand-Saïd, Marie-Elise Lancelot, Aurore Germain, Aline Antonio, Christelle Michiels, Jean-Paul Saraiva, Mélanie Letexier, José-Alain Sahel, Shomi S Bhattacharya, Christina Zeitz


Book ID
119911460
Publisher
BioMed Central
Year
2012
Tongue
English
Weight
551 KB
Volume
7
Category
Article
ISSN
1750-1172

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