Evidence for a common origin of most Friedreich ataxia chromosomes in the Spanish population

European Journal of Human Genetics

Volumn 4, Issue 4, 1996, Pages 191-198

  Monros E ^a  

^a UNIVERSITY OF VALENCIA   (Spain)

Author keywords

Friedreich ataxia; Haplotype divergence analysis

Indexed keywords

ARTICLE; CHROMOSOME; CONTROLLED STUDY; DNA POLYMORPHISM; FRIEDREICH ATAXIA; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MUTATION; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; SPAIN;

ATAXIA;

EID: 0029847764     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1159/000472198     Document Type: Article

References (2)

1. Harding AE : The hereditary ataxias and related disorders. Edinburgh, Churchill Livingstone, 1984.
2. Chamberlain S, Shaw J, Rowland S, Wallis J, South S, Nakamura Y, von Gabain A, et al: Mapping of mutation causing Friedreich ataxia to human chromosome 9. Nature 1988;334:248-250.