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G to A polymorphism in the CACNLG gene.
Olckers A, Jedlicka AE, Powers PA, Hogan K, Gregg RG, Levitt RC. Olckers A, et al. Among authors: hogan k. Hum Mol Genet. 1993 Dec;2(12):2198. doi: 10.1093/hmg/2.12.2198-a. Hum Mol Genet. 1993. PMID: 8111396 No abstract available.
A calcium channel mutation causing hypokalemic periodic paralysis.
Jurkat-Rott K, Lehmann-Horn F, Elbaz A, Heine R, Gregg RG, Hogan K, Powers PA, Lapie P, Vale-Santos JE, Weissenbach J, et al. Jurkat-Rott K, et al. Among authors: hogan k. Hum Mol Genet. 1994 Aug;3(8):1415-9. doi: 10.1093/hmg/3.8.1415. Hum Mol Genet. 1994. PMID: 7987325
Exclusion of malignant hyperthermia susceptibility (MHS) from a putative MHS2 locus on chromosome 17q and of the alpha 1, beta 1, and gamma subunits of the dihydropyridine receptor calcium channel as candidates for the molecular defect.
Sudbrak R, Golla A, Hogan K, Powers P, Gregg R, Du Chesne I, Lehmann-Horn F, Deufel T. Sudbrak R, et al. Among authors: hogan k. Hum Mol Genet. 1993 Jul;2(7):857-62. doi: 10.1093/hmg/2.7.857. Hum Mol Genet. 1993. PMID: 8395939
Refined genetic localization for central core disease.
Mulley JC, Kozman HM, Phillips HA, Gedeon AK, McCure JA, Iles DE, Gregg RG, Hogan K, Couch FJ, MacLennan DH, et al. Mulley JC, et al. Among authors: hogan k. Am J Hum Genet. 1993 Feb;52(2):398-405. Am J Hum Genet. 1993. PMID: 8430700 Free PMC article.
Dinucleotide repeat polymorphism at the D10S178 locus.
Couch FJ, Gregg RG, McCarthy TV, Hogan K. Couch FJ, et al. Among authors: hogan k. Nucleic Acids Res. 1992 Mar 25;20(6):1431. Nucleic Acids Res. 1992. PMID: 1561111 Free PMC article. No abstract available.
Dinucleotide repeat polymorphism at the D10S179 locus.
Couch FJ, McCarthy TV, Hogan K, Gregg RG. Couch FJ, et al. Among authors: hogan k. Nucleic Acids Res. 1992 Mar 25;20(6):1431. Nucleic Acids Res. 1992. PMID: 1561112 Free PMC article. No abstract available.
470 results