Elise Orhan
4PUBLICATIONS
13CO-AUTHORS
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Publications (4)
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|Aug 07, 2021
Mutated <i>CCDC51</i> Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy.Christina Zeitz, Cécile Méjécase, Christelle Michiels
|Apr 30, 2021
A New Mouse Model for Complete Congenital Stationary Night Blindness Due to <i>Gpr179</i> Deficiency.Elise Orhan, Marion Neuillé, Miguel de Sousa Dias
|Mar 22, 2021
Functional expression of complement factor I following AAV-mediated gene delivery in the retina of mice and human cells.Anna K Dreismann, Michelle E McClements, Alun R Barnard
|Oct 30, 2020
WDR34, a candidate gene for non-syndromic rod-cone dystrophy.Maria Solaguren-Beascoa, Kinga M Bujakowska, Cécile Méjécase
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Frequent Collaborators
3 joint publications
Isabelle Audo
3 joint publications
Christina Zeitz
2 joint publications
Cécile Méjécase
2 joint publications
Thierry Léveillard
1 joint publications
Maria Solaguren-Beascoa
1 joint publications
Kinga M Bujakowska
1 joint publications
Saddek Mohand-Saïd
1 joint publications
Hélène Dollfus
1 joint publications
José-Alain Sahel
1 joint publications
Michelle E McClements
