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Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington's disease.

Authors :
Nance MA
Mathias-Hagen V
Breningstall G
Wick MJ
McGlennen RC
Source :
Neurology [Neurology] 1999 Jan 15; Vol. 52 (2), pp. 392-4.
Publication Year :
1999

Abstract

A patient with juvenile Huntington's disease (HD) of probable maternal inheritance is reported. The expanded IT-15 allele was only detected with the use of modified PCR and Southern transfer techniques, which showed a CAG trinucleotide repeat expansion of approximately 250 repeats-the largest CAG expansion reported within the huntingtin gene. This case emphasizes the need for communication between the diagnostic laboratory and the clinician to define the molecular genetics of unusual cases.

Details

Language :
English
ISSN :
0028-3878
Volume :
52
Issue :
2
Database :
MEDLINE
Journal :
Neurology
Publication Type :
Academic Journal
Accession number :
9932964
Full Text :
https://doi.org/10.1212/wnl.52.2.392