Article
A connexin-32 mutation associated with Charcot-Marie-Tooth disease does not affect channel formation in oocytes.
FEBS letters - 29 Aug 1994
Rabadan-Diehl C, Dahl G, Werner R
Abstract excerpt
Members of the connexin family differ most in their carboxy-termini, both with respect to sequence and length. In order to assess the contribution of this region to channel function, a series of carboxy-terminal deletion mutants were tested in the paired-oocyte expression system. Connexin-32 can...
Topics
- Amino Acid Sequence
- Charcot-Marie-Tooth Disease
- Connexins
- Gap Junctions
- Humans
- Molecular Sequence Data
- Mutation
- Oocytes
- Gap Junction beta-1 Protein
