3 results for author:"Pika U." in Literature citations
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| Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linker. Lerche H., Heine R., Pika U., George A.L. Jr., Mitrovic N., Browatzki M., Weiss T., Rivet-Bastide M., Franke C., Lomonaco M. et al. J. Physiol. (Lond.) 470:13-22(1993) · UniProtKB (1) |
| A novel SCN4A mutation causing myotonia aggravated by cold and potassium. Heine R., Pika U., Lehmann-Horn F. Hum. Mol. Genet. 2:1349-1353(1993) · UniProtKB (1) |
| Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletion. Heine R., George A.L. Jr., Pika U., Deymeer F., Ruedel R., Lehmann-Horn F. Hum. Mol. Genet. 3:1123-1128(1994) · UniProtKB (1) |