𝔖 Bobbio Scriptorium
✦   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

No coin nor oath required. For personal study only.