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CLINICAL PRESENTATION AND DISEASE COURSE OF USHER SYNDROME BECAUSE OF MUTATIONS IN MYO7A OR USH2A.
Testa, Francesco; Melillo, Paolo; Bonnet, Crystel; Marcelli, Vincenzo; de Benedictis, Antonella; Colucci, Raffaella; Gallo, Beatrice; Kurtenbach, Anne; Rossi, Settimio; Marciano, Elio; Auricchio, Alberto; Petit, Christine; Zrenner, Eberhart; Simonelli, Francesca.
Affiliation
  • Testa F; *Eye Clinic, Multidisciplinary Department of Medical, Surgical and Dental Sciences, Second University of Naples, Naples, Italy; †Institut de la Vision, UMRS 1120 INSERM/UPMC, Paris, France; ‡Audiology Unit, Department of Neuroscience, Reproductive and Odontostomatologic Sciences, University of Naples Federico II, Naples, Italy; §Centre for Ophthalmology, Institute for Ophthalmic Research, University of Tuebingen, Tuebingen, Germany; ¶Telethon Institute of Genetics and Medicine (TIGEM), Pozzuoli,
Retina ; 37(8): 1581-1590, 2017 Aug.
Article in En | MEDLINE | ID: mdl-27828912
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Full text: 1 Database: MEDLINE Main subject: DNA / Visual Acuity / Visual Fields / Extracellular Matrix Proteins / Myosins / Usher Syndromes / Mutation Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies Limits: Adolescent / Adult / Female / Humans / Male / Middle aged Language: En Journal: Retina Year: 2017 Type: Article
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Full text: 1 Database: MEDLINE Main subject: DNA / Visual Acuity / Visual Fields / Extracellular Matrix Proteins / Myosins / Usher Syndromes / Mutation Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies Limits: Adolescent / Adult / Female / Humans / Male / Middle aged Language: En Journal: Retina Year: 2017 Type: Article