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Patients with Features Similar to Huntington's Disease, Without CAG Expansion in Huntingtin
Neurol 51:215-220, Rosenblatt,A.,et al, 1998
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Article Abstract
Of 15 patients,7 received specific diagnosis or appear to be sporadic cases,4 have a possible but uncertain relation to HD and 4 have unknown familial progressive movement disorders.This last group of patients might be properly described sphenocopies of HD,some of which may be caused by unidentified triplet repeat expansions.
 
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CAG repeats
chorea
chorea,causes of
Huntington's chorea
Huntington's chorea,differential diagnosis
Huntington's chorea,sporadic form
neurologic disease,diagnoses of
trinucleotide repeats

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