Distinct disease mechanisms in peripheral neuropathies due to altered peripheral myelin protein 22 gene dosage or a Pmp22 point mutation

Neurobiology of Disease - Tập 18 - Trang 656-668 - 2005
Guya Giambonini-Brugnoli1, Johanna Buchstaller1, Lukas Sommer1, Ueli Suter1, Ned Mantei1
1Institute for Cell Biology, Department of Biology, ETH-Hönggerberg, Swiss Federal Institute of Technology, Schafmattstrasse 18, CH-8093 Zürich, Switzerland

Tài liệu tham khảo

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