Items where Author is "Wewer, U. M."

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Jump to: 2003 | 1998
Number of items: 2.


Guo, L. T. and Zhang, X. U. and Kuang, W. and Xu, H. and Liu, L. A. and Vilquin, J. -T. and Miyagoe-Suzuki, Y. and Takeda, S. and Ruegg, M. A. and Wewer, U. M. and Engvall, E.. (2003) Laminin alpha2 deficiency and muscular dystrophy : genotype-phenotype correlation in mutant mice. Neuromuscular Disorders, Vol. 13, H. 3. pp. 207-215.


Sieb, J. P. and Dorfler, P. and Tzartos, S. and Wewer, U. M. and Ruegg, M. A. and Meyer, D. and Baumann, I. and Lindemuth, R. and Jakschik, J. and Ries, F.. (1998) Congenital myasthenic syndromes in two kinships with end-plate acetylcholine receptor and utrophin deficiency. Neurology, 50 (1). pp. 54-61.

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