Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1) von KEMP, E. A. M. J. S, HENSELS, G. W, SIE, O. G, DE DIE-SMULDERS, C. E. M, HOOGENDIJK, J. E, DE VISSER, M, BOLHUIS, P. A

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Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot–Marie–Tooth disease type 1B von Kulkens, Tanja, Bolhuis, Pieter A., Wolterman, Ruud A., Kemp, Stephan, te Nijenhuis, Saskia, Valentijn, Linda J., Hensels, Gerard W., Jennekens, Frans G.I., de Visser, Marianne, Hoogendijk, Jessica E., Baas, Frank

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Alternatively sized duplication in Charcot — Marie — Tooth disease type 1A von Valentijn, Linda J., Baas, Frank, Zorn, Ina, Hensels, Gerard W., de Visser, Marianne, Bolhuls, Peter A.

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The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2 von HOOGENDIJK, J. E, HENSELS, G. W, ZORN, I, VALENTIJN, L, JANSSEN, E. A. M, DE VISSER, M, BARKER, D. F, ONGERBOER DE VISSER, B. W, BAAS, F, BOLHUIS, P. A

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The gene for X-linked myotubular myopathy is located in an 8 Mb region at the border of Xq27.3 and Xq28 von Janssen, Emiel A.M., Hensels, Gerard W., van Oost, Bernard A., Hamel, Ben C.J., Kemp, Stephan, Baas, Frank, Weber, Jacobiena W., Barth, Peter G., Bolhuis, Pieter A.

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Deletion of the serine 34 codon from the major peripheral myelin protein P 0 gene in Charcot-Marie-Tooth disease type 1B von Valentijn, Linda J, Kulkens, Tanja, de Visser, Marianne, Baas, Frank, Kemp, Stephan, Hoogendijk, Jessica E, Bolhuis, Pieter A, Jennekens, Frans G.I, Wolterman, Ruud A, te Nijenhuis, Saskia, Hensels, Gerard W

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