A case report of juvenile Huntington disease
Huntington disease (HD) is a progressive neurodegenerative disorder, characterized by autosomal dominant inheritance, movement disorder, dementia, and behavioural disturbances. It is caused by a mutation in IT15 gene on chromosome 4p16.3, which leads to unstable CAG trinucleotide repeat expansion. T...
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Hygeia Press di Corridori Marinella,
2017-09-01T00:00:00Z.
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A1234.567 |
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| Kopya Bilgisi 1 | Kütüphanede |