A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss
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| Description | scientific article |
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author: Peter Charbel Issa Elvir Becirovic Diana Mitter Hendrik Scholl |
| Publication date | December 15, 2006 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |