5 results for author:"Malin J.P." in Literature citations
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| Homozygous mutations in caveolin-3 cause a severe form of rippling muscle disease. Kubisch C., Schoser B.G.H., von Duering M., Betz R.C., Goebel H.-H., Zahn S., Ehrbrecht A., Aasly J., Schroers A., Popovic N. et al. Ann. Neurol. 53:512-520(2003) · UniProtKB (1) |
| Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease. Betz R.C., Schoser B.G.H., Kasper D., Ricker K., Ramirez A., Stein V., Torbergsen T., Lee Y.-A., Nothen M.M., Wienker T.F. et al. Nat. Genet. 28:218-219(2001) · UniProtKB (1) |
| Novel missense mutations in the glycogen-branching enzyme gene in adult polyglucosan body disease. Ziemssen F., Sindern E., Schroder J.M., Shin Y.S., Zange J., Kilimann M.W., Malin J.P., Vorgerd M. Ann. Neurol. 47:536-540(2000) · UniProtKB (1) |
| Adult-onset glycogen storage disease type II: phenotypic and allelic heterogeneity in German patients. Vorgerd M., Burwinkel B., Reichmann H., Malin J.-P., Kilimann M.W. Neurogenetics 1:205-211(1998) · UniProtKB (1) |
| Mutation analysis in myophosphorylase deficiency (McArdle's disease). Vorgerd M., Kubisch C., Burwinkel B., Reichmann H., Mortier W., Tettenborn B., Pongratz D., Lindemuth R., Tegenthoff M., Malin J.P. et al. Ann. Neurol. 43:326-331(1998) · UniProtKB (1) |