The structure of the gene encoding the human skeletal muscle α1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3)

Genomics

Volumn 31, Issue 3, 1996, Pages 392-394

  Hogan, Kirk ^a,c   Gregg, Ronald G ^b   Powers, Patricia A ^a,b  

^a UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

^b UNIVERSITY OF WISCONSIN MADISON   (United States)

^c University of Wisconsin Health   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL; CALCIUM ION; COMPLEMENTARY DNA; DIHYDROPYRIDINE;

ALPHA CHAIN; ARTICLE; DNA SEQUENCE; EXON; GENE STRUCTURE; HUMAN; INTRON; PRIORITY JOURNAL; SKELETAL MUSCLE;

EID: 0030064359     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0066     Document Type: Article

References (12)

1. Birnbaumer, L., Campbell, K. P., Catterall, W. A., Harpold, M. M., Hofmann, F., Horne, W. A., Mori, Y., Schwartz, A., Snutch, T. P., Tanabe, T., and Tsien, R. W. (1994). The naming of voltage-gated calcium channels. Neuron 13: 505-506.
2. Devereaux, J., Haeberli, P., and Smithies, O. (1984). A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. 12: 387-395.
3. Fontaine, B., Vale-Santos, J., Jurkat-Rott, K., Reboul, E., Plassart, E., Rime, C.-S., Elbaz, A., Heine, R., Guimaraes, J., Weissenbach, J., Baumann, N., Fardeau, M., and Lehmann-Horn, F. (1994). Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families. Nature Genet. 6: 267-272.
4. 2+ channel (CACHL1A3) to chromosome 1q31-32. Genomics 15: 107-112.
5. 1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3). Genomics 24: 608-609.
6. 1-subunit of the skeletal muscle L-type voltage-dependent calcium channel (CACNL1A3) to human chromosome 1q32 by in situ hybridization. Genomics 19: 561-563.
7. Isom, L. L., DeJongh, K. S., and Catterall, W. A. (1994). Auxilary subunits of voltage-gated ion channels. Neuron 12: 1183-1194.
8. Jurkat-Rott, K., Lehmann-Horn, F., Elbaz, A., Heine, R., Gregg, R. G., Powers, P. A., Hogan, K., Lapie, P., Vale-Santos, J., Weissenbach, J., and Fontaine, B. (1994). A calcium channel mutation causing hypokalemic periodic paralysis. Hum. Mol. Genet. 3: 1415-1419.
9. 1 subunit from the dihydropyridine receptor of skeletal muscle. Nature 340: 233-236.
10. Ptacek, L. J., Tawil, R., Griggs, R. C., Engel, A. G., Layzer, R. B., Kwiecinski, H., McManis, P. G., Santiago, L., Moore, M., Fouad, G., Bradley, P., and Leppert, M. F. (1994). Dihydropyridine receptor mutations cause hypokalemic periodic paralysis. Cell 77: 863-868.
11. 2+ channel. Genomics 22: 77-87.
12. 1 subunit (CACNL1A2) and β subunit (CACNLB3) genes. Genomics 27: 312-319.