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Cancer: From Wild-Type to Mutant Huntingtin

Huntingtin (HTT) is a scaffold protein mostly known because it gives rise to the severe and incurable inherited neurological disorder Huntington’s disease (HD) when mutated. The Huntingtin gene (HTT) carries a polymorphic trinucleotide expansion of CAGs in exon 1 that ranges from 9 to 35 in the non-...

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Detalhes bibliográficos
Publicado no:J Huntingtons Dis
Main Authors: Thion, Morgane Sonia, Humbert, Sandrine
Formato: Artigo
Idioma:Inglês
Publicado em: IOS Press 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6087435/
https://ncbi.nlm.nih.gov/pubmed/29889077
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JHD-180290
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