The GAA Triplet-Repeat Expansion in Friedreich Ataxia Interferes with Transcription and May Be Associated with an Unusual DNA Structure-Reference-Cited by-同舟云学术

The GAA Triplet-Repeat Expansion in Friedreich Ataxia Interferes with Transcription and May Be Associated with an Unusual DNA Structure

Published:1998-01 Issue:1 Volume:62 Page:111-121
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Bidichandani Sanjay I.,Ashizawa Tetsuo,Patel Pragna I.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference48 articles.

1. Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin;Babcock;Science.,1997

2. Recessive ataxia in Acadians and Cajuns;Barbeau;Can J Neurol Sci,1984

3. Structural polymorphism of homopurine-homopyrimidine sequences: the secondary DNA structure adopted by a d(GA•CT)22 sequence in the presence of zinc ions;Bernués;EMBO J,1989

4. Atypical Friedreich ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion;Bidichandani;Am J Hum Genet,1997

5. Transcriptional suppression in Friedreich ataxia: consequences of the intronic GAA triplet repeat expansion;Bidichandani;Am J Hum Genet,1996

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