DIANA
VALVERDE PEREZ
CATEDRATICO/A DE UNIVERSIDAD TC
Guillermo
Antiñolo Gil
Publications by the researcher in collaboration with Guillermo Antiñolo Gil (7)
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
2007
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Spectrum of the ABCA4 gene mutations implicated in severe retinopathies in Spanish patients
Investigative Ophthalmology and Visual Science, Vol. 48, Núm. 3, pp. 985-990
2006
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Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II.
Journal of medical genetics, Vol. 43, Núm. 11
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Mutation profile of the MYO7A gene in Spanish patients with Usher syndrome type I.
Human mutation, Vol. 27, Núm. 3, pp. 290-291
2005
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Sequence variations in the retinal fascin FSCN2 gene in a Spanish population with autosomal dominant retinitis pigmentosa or macular degeneration
Molecular Vision, Vol. 11, pp. 922-928
1995
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Retinitis pigmentosa in Spain
Clinical Genetics, Vol. 48, Núm. 3, pp. 120-122