Genetic recombination events which position the friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9q

The absence of recombination between the mutation causing Friedreich ataxia and the two loci which originally assigned the disease locus to chromosome 9 has slowed attempts to isolate and characterize the genetic defect underlying this neurodegenerative disorder. A proximity of less than 1 cM to the...

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Hlavní autoři: Chamberlain, Susan, Farrall, Martin, Shaw, Jacqui, Wilkes, David, Carvajal, Jaime, Hillerman, Renate, Doudney, Kit, Harding, A. E., Williamson, Robert, Sirugo, Giorgio, Fujita, Ricardo, Koenig, Michel, Mandel, Jean-Louis, Palau, Francisco, Monros, Eugenia, Vilchez, Juan, Prieto, Felix, Richter, Andrea, Vanasse, Michel, Melancon, Serge, Cocozza, Sergio, Redolfi, Elena, Cavalcanti, Francesca, Pianese, Luigi, Filla, Allesandro, DiDonato, Stefano, Pandolfo, Massimo
Médium: Artigo
Jazyk:Inglês
Vydáno: 1993
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Original Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682111/
https://ncbi.nlm.nih.gov/pubmed/8434613
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