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An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

✍ Scribed by Meindl, Alfons; Strom, Tim M.; Nyakatura, Gerald; Apfelstedt-Sylla, Eckart; Hellebrand, Heide; Lorenz, Birgit; Weber, Bernhard H. F.; Wutz, Krisztina; Gutwillinger, Nadja; Rüther, Klaus; Drescher, Bernd; Sauer, Christian; Zrenner, Eberhart; Meitinger, Thomas; Rosenthal, Andre


Book ID
109832126
Publisher
Nature Publishing Group
Year
1998
Tongue
English
Weight
455 KB
Volume
19
Category
Article
ISSN
1061-4036

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