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

The recent cloning of cDNA encoding the Ca(++) release channel (ryanodine receptor) of human sarcoplasmic reticulum has enabled us to use somatic cell hybrids to localize the ryanodine receptor gene (RYR) to the proximal long arm of human chromosome 19. Studies with additional hybrids containing del...

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Autores principales: MacKenzie, Alex E., Korneluk, Robert G., Zorzato, Francesco, Fujii, Junichi, Phillips, Michael, Iles, David, Wieringa, Bé, Leblond, Suzanne, Bailly, Jane, Willard, Huntington F., Duff, Catherine, Worton, Ronald G., MacLennan, David H.
Formato: Artigo
Lenguaje:Inglês
Publicado: 1990
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Original Articles
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683814/
https://ncbi.nlm.nih.gov/pubmed/1971150
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