✦ LIBER ✦
Functional analysis of human CNGA3 mutations associated with colour blindness suggests impaired surface expression of channel mutants A3R427C and A3R563C
✍ Scribed by Katja Koeppen; Peggy Reuter; Susanne Kohl; Britta Baumann; Thomas Ladewig; Bernd Wissinger
- Book ID
- 109027437
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 621 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0953-816X
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