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

• Main Authors: Lobato Ana (Author), Sand Jette C (Author), Braathen Geir J (Author), Høyer Helle (Author), Russell Michael B (Author)
• Format: Book
• Published: BMC, 2010-03-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Point mutations in the <it>mitofusin 2 </it>(<it>MFN2</it>) gene has been identified exclusively in Charcot-Marie-Tooth type 2 (CMT2), and in a single family with intermediate CMT. <it>MFN2 </it>po...