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. 1991 Sep 25;19(18):5094. doi: 10.1093/nar/19.18.5094

Dinucleotide repeat polymorphism at the RYR1 locus (19q13.1)

FJ Couch ^1,², K Hogan ¹, TV McCarthy ², RG Gregg ¹

PMCID: PMC328839 PMID: 1923791

Abstract

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

MacKenzie A. E., Korneluk R. G., Zorzato F., Fujii J., Phillips M., Iles D., Wieringa B., Leblond S., Bailly J., Willard H. F. The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy. Am J Hum Genet. 1990 Jun;46(6):1082–1089. [PMC free article] [PubMed] [Google Scholar]
Zorzato F., Fujii J., Otsu K., Phillips M., Green N. M., Lai F. A., Meissner G., MacLennan D. H. Molecular cloning of cDNA encoding human and rabbit forms of the Ca2+ release channel (ryanodine receptor) of skeletal muscle sarcoplasmic reticulum. J Biol Chem. 1990 Feb 5;265(4):2244–2256. [PubMed] [Google Scholar]

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