DOI:
10.1055/s-00000004
Aktuelle Neurologie
LinksClose Window
References
Shy ME, Siskind C, Swan ER et al.
CMT1X phenotypes represent loss of GJB1 gene function.
Neurology 2007;
68: 849-855
Search in:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.