HERMINIO
PEREZ GARRIGUES
TITULAR DE UNIVERSIDAD
E.
Aller
Publications dans lesquelles il/elle collabore avec E. Aller (6)
2010
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Novel mutations in the USH1C gene in Usher syndrome patients
Molecular Vision, Vol. 16, pp. 2948-2954
2007
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MYO7A mutation screening in Usher syndrome type I patients from diverse origins.
Journal of medical genetics, Vol. 44, Núm. 3
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Screening of the USH1G gene among Spanish patients with usher syndrome. Lack of mutations and evidence of a minor role in the pathogenesis of the syndrome
Ophthalmic Genetics, Vol. 28, Núm. 3, pp. 151-155
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
2004
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Genetic analysis of 2299delG and C759F mutations (USH2A) in patients with visual and/or auditory impairments
European Journal of Human Genetics, Vol. 12, Núm. 5, pp. 407-410