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

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Loss of phosphatase activity in myotubularin-related protein 2 is associated with Charcot–Marie–Tooth disease type 4B1

By Berger P.  

Human Molecular Genetics, Vol. 11, Iss. 13, 2002-06 ,pp. : 1569-1579

Oxford University Press

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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

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Reversal of neuropathy phenotypes in conditional mouse model of CharcotMarieTooth disease type 2E

By Dequen Florence   Filali Mohammed   Larivire Roxanne C.   Perrot Rodolphe   Hisanaga Shin-Ichi   Julien Jean-Pierre  

Human Molecular Genetics, Vol. 19, Iss. 13, 2010-07 ,pp. : 2616-2629

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Autosomal Dominant Charcot-Marie-Tooth Axonal Neuropathy Mapped on Chromosome 7p (CMT2D)

By Ionasescu Victor   Searby Charles   Sheffield Val C.   Roklina Tatiana   Nishimura Darrell   Ionasescu Rebecca  

Human Molecular Genetics, Vol. 5, Iss. 9, 1996-01 ,pp. : 1373-1375

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