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Therapeutic Strategies in Huntington’s Disease: From Genetic Defect to Gene Therapy

Despite the identification of an expanded CAG repeat on exon 1 of the huntingtin gene located on chromosome 1 as the genetic defect causing Huntington’s disease almost 30 years ago, currently approved therapies provide only limited symptomatic relief and do not influence the age of onset or disease...

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Autori principali: Anamaria Jurcau, Maria Carolina Jurcau
Natura: Artigo
Lingua:Inglês
Pubblicazione: MDPI AG 2022-08-01
Serie:Biomedicines
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Accesso online:https://www.mdpi.com/2227-9059/10/8/1895
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