ProjectSNPs in SCA3 – Identification of disease-associated single nucleotide polymorphisms in ataxin-3

Basic data

Acronym:
SNPs in SCA3
Title:
Identification of disease-associated single nucleotide polymorphisms in ataxin-3
Duration:
02/05/2024 to 01/08/2024
Abstract / short description:
This project aims to identify single nucleotide polymorphisms (SNPs) associated with the cytosine-adenine-guanine (CAG) trinucleotide repeat expansion that causes spinocerebellar ataxia type 3 (SCA3) in order to develop an allele-specific therapeutic approach using antisense olionucleotides (ASOs).

Involved staff

Managers

University Department of Neurology
Hospitals and clinical institutes, Faculty of Medicine

Contact persons

University Department of Neurology
Hospitals and clinical institutes, Faculty of Medicine

Local organizational units

Department of Neurology with Focus on Neurodegenerative Disorders
University Department of Neurology
Hospitals and clinical institutes, Faculty of Medicine

Funders

London, United Kingdom
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