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Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2011, Volume 6, Issue 1, pp. 21 - 21
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2018, Volume 13, Issue 6, pp. e0199048 - e0199048
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 05/2016, Volume 61, Issue 5, pp. 419 - 422
Journal Article
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 07/2016, Volume 37, Issue 3, pp. 328 - 330
Journal Article
Acta otorrinolaringologica espanola, ISSN 0001-6519, 08/2005, Volume 56, Issue 7, p. 285
Usher syndrome (USH) associates deafness and retinitis pigmentosa (RP). It is a disease both clinically and genetically heterogeneous. It is inherited as an... 
Usher Syndromes - therapy | Prevalence | Usher Syndromes - genetics | Spain - epidemiology | Usher Syndromes - epidemiology | Humans | Molecular Biology - methods | Genetic Therapy - methods
Journal Article
Boletín de la Asociación Médica de Puerto Rico, ISSN 0004-4849, 10/2010, Volume 102, Issue 4, pp. 54 - 58
Journal Article