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Extending the Phenotypic Spectrum of Huntington Disease: Hypothermia

Huntington disease (HD) is an autosomal dominant progressive neurodegenerative disorder associated with expanded CAG repeat size in the huntingtin gene and usually presenting with movement disorder, psychiatric symptoms, and cognitive decline. Sleep problems, weight loss, and cachexia are also commo...

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Bibliografiske detaljer
Udgivet i:Mol Syndromol
Main Authors: Altıner, Şule, Ardic, Senol, Çebi, Alper H.
Format: Artigo
Sprog:Inglês
Udgivet: S. Karger AG 2020
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7109404/
https://ncbi.nlm.nih.gov/pubmed/32256303
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000505887
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