Two novel missense mutations in the myelin protein zero gene causes Charcot-Marie-Tooth type 2 and Déjérine-Sottas syndrome

by Sand Jette C, Braathen Geir J, Russell Michael B
Published 2010-04-01

Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth disease

by Sand Jette C, Braathen Geir J, Bukholm Geir, Russell Michael B
Published 2007-07-01

<it>MFN2 </it>point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT families

by Lobato Ana, Sand Jette C, Braathen Geir J, Høyer Helle, Russell Michael B
Published 2010-03-01