Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosis

Neuromuscular Disorders - Tập 15 - Trang 764-767 - 2005
E. Mikešová1, K. Hühne2, B. Rautenstrauss2, R. Mazanec3, L. Baránková3, M. Vyhnálek3, O. Horáček4, P. Seeman1
1Department of Child Neurology, 2nd School of Medicine, Charles University Prague, V Úvalu 84, 15006 Prague, Czech Republic
2Institut für Humangenetik der Universität Erlangen-Nürnberg, Schwabachanlage 10, D-91054 Erlangen, Germany
3Department of Neurology, 2nd School of Medicine, Charles University Prague, V Úvalu 84, 15006 Prague, Czech Republic
4Department of Rehabilitation, 2nd School of Medicine, Charles University Prague, V Úvalu 84, 15006 Prague, Czech Republic

Tài liệu tham khảo

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