Showing results 1 to 2 of 2
Title | Author(s) | Issue Date | |
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Pathogenetic role of the deafness-related M34T mutation of Cx26 Journal:Human Molecular Genetics | 2006 | ||
Selective defects in channel permeability associated with Cx32 mutations causing X-linked Charcot-Marie-Tooth disease Journal:Neurobiology of Disease | 2006 |