Usher syndrome: Clinical features, diagnostic options, and therapeutic prospects
Usher syndrome denotes a clinically and genetically heterogeneous combination of retinitis pigmentosa and sensorineural deafness. The division into subtypes I, II, and III is based on the degree of hearing loss: Type I is characterized by deafness from birth together with ataxia and retarded motor d...
| Päätekijät: | , , |
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| Aineistotyyppi: | Journal article |
| Kieli: | German |
| Julkaistu: |
2009
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