Open AccessDiagnosis of Huntington Disease
Author(s) -
Russell L. Margolis,
Christopher A. Ross
Publication year - 2003
Publication title -
clinical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.705
H-Index - 218
eISSN - 1530-8561
pISSN - 0009-9147
DOI - 10.1373/49.10.1726
Subject(s) - etiology , disease , huntington's disease , asymptomatic , genetic counseling , genetic testing , predictive testing , trinucleotide repeat expansion , medicine , pediatrics , presentation (obstetrics) , diagnostic test , pathology , genetics , biology , surgery , allele , gene
Huntington disease (HD) is a rare, progressive, and fatal autosomal dominant neurodegenerative disorder, typically of adult onset.
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