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Research | | Open
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients
- christine.petit@pasteur.fr
- Crystel Bonnet
- , Zied Riahi
- , Sandra Chantot-Bastaraud
- , Luce Smagghe
- , Mélanie Letexier
- , Charles Marcaillou
- , Gaëlle M Lefèvre
- , Jean-Pierre Hardelin
- , Aziz El-Amraoui
- , Amrit Singh-Estivalet
- , Saddek Mohand-Saïd
- , Susanne Kohl
- , Anne Kurtenbach
- , Ieva Sliesoraityte
- , Ditta Zobor
- , Souad Gherbi
- , Francesco Testa
- , Francesca Simonelli
- , Sandro Banfi
- , Ana Fakin
- , Damjan Glavač
- , Martina Jarc-Vidmar
- , Andrej Zupan
- , Saba Battelino
- , Loreto Martorell Sampol
- , Maria Antonia Claveria
- , Jaume Catala Mora
- , Shzeena Dad
- , Lisbeth B Møller
- , Jesus Rodriguez Jorge
- , Marko Hawlina
- , Alberto Auricchio
- , José-Alain Sahel
- , Sandrine Marlin
- , Eberhart Zrenner
- , Isabelle Audo
- & Christine Petit
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Reviews |
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Research | | Open
