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Monique Cordonnier

Showing results (11-20 of 14) with videos related to

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Ophthalmic Genetics|May 8, 2019
Identification of a novel GRM6 mutation in a previously described consanguineous family with complete congenital stationary night blindnessAurore Tourville, Christelle Michiels, Christel Condroyer, et al.
Journal of Child Neurology|July 19, 2013
Uncommon Leber "plus" disease associated with mitochondrial mutation m.11778G>A in a premature childStéphanie Paquay, Valérie Benoit, Catherine Wetzburger, et al.
International Journal of Molecular Sciences|June 24, 2022
Novel <i>OPN1LW/OPN1MW</i> Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone DysfunctionKatarina Stingl, Britta Baumann, Pietro De Angeli, et al.
The Lancet. Neurology|September 30, 2022
Diagnosis and classification of optic neuritisAxel Petzold, Clare L Fraser, Mathias Abegg, et al.
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Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Ophthalmic Genetics|May 8, 2019
Identification of a novel GRM6 mutation in a previously described consanguineous family with complete congenital stationary night blindnessAurore Tourville, Christelle Michiels, Christel Condroyer, et al.
Journal of Child Neurology|July 19, 2013
Uncommon Leber "plus" disease associated with mitochondrial mutation m.11778G>A in a premature childStéphanie Paquay, Valérie Benoit, Catherine Wetzburger, et al.
International Journal of Molecular Sciences|June 24, 2022
Novel <i>OPN1LW/OPN1MW</i> Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone DysfunctionKatarina Stingl, Britta Baumann, Pietro De Angeli, et al.
The Lancet. Neurology|September 30, 2022
Diagnosis and classification of optic neuritisAxel Petzold, Clare L Fraser, Mathias Abegg, et al.
Pageof 2