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...
| Hlavní autoři: | , , |
|---|---|
| Médium: | Journal article |
| Jazyk: | German |
| Vydáno: |
2009
|