4 results for author:"Sloan-Brown K." in Literature citations
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| A novel muscle sodium channel mutation causes painful congenital myotonia. Rosenfeld J., Sloan-Brown K., George A.L. Jr. Ann. Neurol. 42:811-814(1997) · UniProtKB (1) |
| Nonsense and missense mutations of the muscle chloride channel gene in patients with myotonia congenita. George A.L. Jr., Sloan-Brown K., Fenichel G.M., Mitchell G.A., Spiegel R., Pascuzzi R.M. Hum. Mol. Genet. 3:2071-2072(1994) · UniProtKB (1) |
| Genomic organization and chromosomal assignment of the human voltage-gated Na+ channel beta 1 subunit gene (SCN1B). Makita N., Sloan-Brown K., Weghuis D.O., Ropers H.-H., George A.L. Jr. Genomics 23:628-634(1994) · UniProtKB (1) |
| Translational activation of the non-AUG-initiated c-myc 1 protein at high cell densities due to methionine deprivation. Hann S.R., Sloan-Brown K., Spotts G.D. Genes Dev. 6:1229-1240(1992) · UniProtKB (1) |