Charcot-Marie-Tooth disease and related peripheral neuropathies: novel mutations in the peripheral myelin genes connexin 32 (Cx32 ), peripheral myelin protein 22 (PMP22 ), and peripheral myelin protein zero (MPZ )

Neurogenetics - Tập 3 - Trang 49-50 - 2000
A. B. Ekici1, D. Schweitzer1, O. Park1, D. Lorek1, B. Rautenstrauss1, G. Krüger2, W. Friedl3, S. Uhlhaas3, K. Bathke4, D. Heuss4, C. Kayser4, H. Grehl5
1Institute of Human Genetics, University of Erlangen-Nuernberg, 91054 Erlangen, Germany e-mail: [email protected] Tel.: +49-9131-8522352 Fax: +49-9131-209297, , DE
2Department of Medical Genetics, Rostock, Germany, , DE
3Institute of Human Genetics, Bonn, Germany, , DE
4Department of Neurology, University of Erlangen-Nuernberg, Erlangen, Germany, , DE
5Department of Neurology, Duisburg, Germany, , DE

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Neurogenetics

Tập 3

49-50

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