Title : The differential diagnosis of Huntington's disease-like syndromes: 'red flags' for the clinician.

Pub. Date : 2013 Jun

PMID : 22993450






1 Functional Relationships(s)
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1 Differentiating among these HD-like syndromes is necessary when a patient with a combination of movement disorders, cognitive decline, behavioural abnormalities and progressive disease course proves negative to the genetic testing for HD causative mutations, that is, IT15 gene trinucleotide-repeat expansion. trinucleotide huntingtin Homo sapiens