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Navegación por Autor Orhan, Elise
Mostrando resultados 1 a 3 de 3
Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
closedAccess | | dic-2013 | Further insights into GPR179: Expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindness | Orhan, Elise; Bhattacharya, Shom Shanker CSIC ORCID; Zeitz, Christina | artículo |
closedAccess | | ene-2012 | RP1 and autosomal dominant rod-cone dystrophy: Novel mutations, a review of published variants, and genotype-phenotype correlation | Audo, Isabelle; Orhan, Elise; Bhattacharya, Shom Shanker CSIC ORCID; Zeitz, Christina | artículo |
closedAccess | | feb-2021 | WDR34, a candidate gene for non-syndromic rod-cone dystrophy | Solaguren-Beascoa, María; Bujakowska, Kinga; Méjécase, Cécile; Emmenegger, Lisa; Orhan, Elise; Neuillé, Marion; Mohand-Saïd, Saddek; Condroyer, Christel; Lancelot, Marie-Elise; Michiels, Christelle; Demontant, Vanessa; Antonio, Aline; Letexier, Mélanie; Saraiva, Jean-Paul; Lonjou, Christine; Carpentier, Wassila; Léveillard, Thierry; Pierce, Eric A.; Dollfus, Hélène; Sahel, José-Alain; Bhattacharya, Shom Shanker CSIC ORCID; Audo, Isabelle; Zeitz, Christina | artículo |