✦ LIBER ✦
A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss
✍ Scribed by Inga Ebermann; Hendrik P. N. Scholl; Peter Charbel Issa; Elvir Becirovic; Jürgen Lamprecht; Bernhard Jurklies; José M. Millán; Elena Aller; Diana Mitter; Hanno Bolz
- Publisher
- Springer
- Year
- 2006
- Tongue
- English
- Weight
- 518 KB
- Volume
- 121
- Category
- Article
- ISSN
- 0340-6717
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