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Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases. [electronic resource] by
- Audo, Isabelle
- Bujakowska, Kinga M
- Léveillard, Thierry
- Mohand-Saïd, Saddek
- Lancelot, Marie-Elise
- Germain, Aurore
- Antonio, Aline
- Michiels, Christelle
- Saraiva, Jean-Paul
- Letexier, Mélanie
- Sahel, José-Alain
- Bhattacharya, Shomi S
- Zeitz, Christina
Producer: 20120828
In:
Orphanet journal of rare diseases vol. 7
Availability: No items available.
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