Related content

An animal model for Charcot–Marie–Tooth disease type 4B1

By Bonneick Sonja   Boentert Matthias   Berger Philipp   Atanasoski Suzana   Mantei Ned   Wessig Carsten   Toyka Klaus V.   Young Peter   Suter Ueli  

Human Molecular Genetics, Vol. 14, Iss. 23, 2005-12 ,pp. : 3685-3695

Oxford University Press

Access to resources Recommend Favorite

GDAP1, the protein causing Charcot–Marie–Tooth disease type 4A, is expressed in neurons and is associated with mitochondria

By Pedrola Laia  

Human Molecular Genetics, Vol. 14, Iss. 8, 2005-04 ,pp. : 1087-1094

Oxford University Press

Access to resources Recommend Favorite

Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot–Marie–Tooth neuropathy type 4B2/11p15

By Senderek J.  

Human Molecular Genetics, Vol. 12, Iss. 3, 2003-02 ,pp. : 349-356

Oxford University Press

Access to resources Recommend Favorite

Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot–Marie–Tooth neuropathy type 4B2/11p15

By Senderek Jan   Bergmann Carsten   Weber Susanne   Ketelsen Uwe-Peter   Schorle Hubert   Rudnik-Schöneborn Sabine   Büttner Reinhard   Buchheim Eckhard   Zerres Klaus  

Human Molecular Genetics, Vol. 13, Iss. 3, 2004-02 ,pp. : 363-363

Oxford University Press

Access to resources Recommend Favorite

Multi-level regulation of myotubularin-related protein-2 phosphatase activity by myotubularin-related protein-13/set-binding factor-2

By Berger Philipp   Berger Imre   Schaffitzel Christiane   Tersar Kristian   Volkmer Benjamin   Suter Ueli  

Human Molecular Genetics, Vol. 15, Iss. 4, 2006-02 ,pp. : 569-579

Oxford University Press

Access to resources Recommend Favorite