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Functional Analysis of a Dominant Mutation of Human Connexin26 Associated with Nonsyndromic Deafness

✍ Scribed by Bruzzone, R.; Gomès, D.; Denoyelle, F.; Duval, N.; Perea, J.; Veronesi, V.; Weil, D.; Petit, C.; Gabellec, M.-M.; D'andrea, P.; White, T. W.


Book ID
120297543
Publisher
Informa plc
Year
2001
Tongue
English
Weight
556 KB
Volume
8
Category
Article
ISSN
1541-9061

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