Genetic Testing in Huntington’s Disease

J Gordon Millichap

doi:10.15844/pedneurbriefs-11-11-9

Genetic Testing in Huntington’s Disease

Pediatric Neurology Briefs

Volume 11 (1997): Issue 11

By: J Gordon Millichap

Open Access

|Nov 1997

Abstract

The historical and clinical profiles of Huntington’s disease (HD) presenting in 44 juveniles who were tested for CAG repeat expansions in the gene for HD were defined in a study reported by the US Huntington Disease Genetic Testing Group from the Hennepin County Medical Center, Minneapolis, MN.

References

Nance MA US Huntington Disease Genetic Testing Group Genetic testing of children at risk for Huntington’s disease Neurology 1997 Oct 49 4 1048 1053 10.1212/WNL.49.4.1048 9339688
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Almqvist E Adam S Bloch M Fuller A Welch P Eisenberg D Risk reversals in predictive testing for Huntington disease Am J Hum Genet 1997 Oct 61 4 945 952 10.1086/514873 9382108
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-11-11-9 | Journal eISSN: 2166-6482

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Language: English

Page range: 87 - 87

Published on: Nov 1, 1997

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Huntington’s disease,

Genetic Testing,

Gait Disorder

© 1997 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 11 (1997): Issue 11