Evolution of the Friedreich's ataxia trinucleotide repeat expansion: Founder effect and premutations

Proceedings of the National Academy of Sciences of the United States of America

Volumn 94, Issue 14, 1997, Pages 7452-7457

  Cossée, Mireille ^a   Schmitt, Michèle ^b   Campuzano, Victoria ^a   Reutenauer, Laurence ^a   Moutou, Céline ^b   Mandel, Jean Louis ^a   Koenig, Michel ^a  

^a INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

^b UNIVERSITÉ DE STRASBOURG   (France)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT;

ALLELE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CONTROLLED STUDY; FRAGILE X SYNDROME; FRIEDREICH ATAXIA; GENE MUTATION; GENETIC POLYMORPHISM; HUMAN; INTRON; MAJOR CLINICAL STUDY; MYOTONIC DYSTROPHY; PRIORITY JOURNAL; TRINUCLEOTIDE REPEAT;

ALLELES; FEMALE; FOUNDER EFFECT; FRIEDREICH ATAXIA; HUMANS; MALE; POLYMORPHISM, GENETIC; TRINUCLEOTIDE REPEATS;

ATAXIA;

EID: 0030739437     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.94.14.7452     Document Type: Article

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