ELENA
VALLESPÍN GARCÍA
Investigadora hasta 2022
Marta
Cortón Pérez
Publicaciones en las que colabora con Marta Cortón Pérez (6)
2021
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Author Correction: Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications (Scientific Reports, (2021), 11, 1, (1526), 10.1038/s41598-021-81093-y)
Scientific Reports
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Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications
Scientific Reports, Vol. 11, Núm. 1
2017
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Improving molecular diagnosis of aniridia and WAGR syndrome using customized targeted array-based CGH
PLoS ONE, Vol. 12, Núm. 2
2014
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Involvement of LCA5 in leber congenital amaurosis and retinitis pigmentosa in the Spanish population
Ophthalmology, Vol. 121, Núm. 1, pp. 399-407
2013
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High frequency of CRB1 mutations as cause of Early-Onset Retinal Dystrophies in the Spanish population
Orphanet Journal of Rare Diseases, Vol. 8, Núm. 1
2010
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Mutation analysis of 272 Spanish families affected by autosomal recessive retinitis pigmentosa using a genotyping microarray
Molecular Vision, Vol. 16, pp. 2550-2558