Charcot–Marie–Tooth disease CMT4A: GDAP1 increases cellular glutathione and the mitochondrial membrane potential

By Noack Rebecca   Frede Svenja   Albrecht Philipp   Henke Nadine   Pfeiffer Annika   Knoll Katrin   Dehmel Thomas   Meyer zu Hörste Gerd   Stettner Mark   Kieseier Bernd C.   Summer Holger   Golz Stefan   Kochanski Andrzej   Wiedau-Pazos Martina   Arnold Susanne   Lewerenz Jan   Methner Axel  

Human Molecular Genetics, Vol. 21, Iss. 1, 2012-01 ,pp. : 150-162

Oxford University Press

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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

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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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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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A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24

By Tang Bei-sha   Luo Wei   Xia Kun   Xiao Jian-feng   Jiang Hong   Shen Lu   Tang Jian-guang   Zhao Guo-hua   Cai Fang   Pan Qian   Dai He-ping   Yang Qi-dong   Xia Jia-hui   Evgrafov Oleg  

Human Genetics, Vol. 114, Iss. 6, 2004-05 ,pp. : 527-533

Springer Publishing Company

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