Friedreich ataxia in Italian families: Genetic homogeneity and linkage disequilibrium with the marker loci D9S5 and D9S15

Friedreich ataxia (FA) is an autosomal recessive degenerative disease of the nervous system of unknown biochemical cause. The FA gene has been shown to be in close linkage with the two chromosome 9 markers D9S5 and D9S15, and linkage disequilibrium between FA and D9S15 has been detected in French fa...

全面介紹

Na minha lista:
書目詳細資料
Main Authors: Pandolfo, Massimo, Sirugo, Giorgio, Antonelli, Antonella, Weitnauer, Leonor, Ferretti, Luca, Leone, Maurizio, Dones, Ivano, Cerino, Antonella, Fujita, Ricardo, Hanauer, Andre, Mandel, Jean-Louis, Di Donato, Stefano
格式: Artigo
語言:Inglês
出版: 1990
主題:
Original Articles
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683703/
https://ncbi.nlm.nih.gov/pubmed/2378348
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!

相似書籍