Showing results 1 to 2 of 2
Title | Author(s) | Issue Date | |
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Connexin32 in the peripheral nervous system: Functional analysis of mutations associated with X-linked Charcot-Marie-Tooth syndrome and implications for the pathophysiology of the disease Journal:Annals of the New York Academy of Sciences | 1999 | ||
Functional analysis of a dominant mutation of human connexin26 associated with nonsyndromic deafness Journal:Cell Communication and Adhesion | 2001 |