Reply to: Comment to “SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies”

Author:

Rudaks Laura Ivete1234ORCID,Yeow Dennis12356ORCID,Kumar Kishore Raj12378

Affiliation:

1. Molecular Medicine Laboratory and Neurology Department Concord Repatriation General Hospital Concord New South Wales Australia

2. Faculty of Medicine and Health The University of Sydney Camperdown New South Wales Australia

3. Translational Neurogenomics Group, Genomic and Inherited Disease Program The Garvan Institute of Medical Research Darlinghurst New South Wales Australia

4. Clinical Genetics Unit Royal North Shore Hospital St Leonards New South Wales Australia

5. Neurodegenerative Service Prince of Wales Hospital Randwick New South Wales Australia

6. Neuroscience Research Australia Randwick New South Wales Australia

7. Faculty of Medicine St Vincent's Healthcare Campus, St Vincent's Hospital Darlinghurst New South Wales Australia

8. St Vincent's Healthcare Campus, Faculty of Medicine UNSW Sydney Darlinghurst New South Wales Australia

Publisher

Wiley

Reference7 articles.

1. Comment to: “SCA4 unravelled after more than 25 years using advanced genomic technologies;Paucar M;Mov Disord,2024

2. SCA4 unravelled after more than 25 years using advanced genomic technologies;Rudaks LI;Mov Disord,2024

3. Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: a poly‐glycine disease;Wallenius J;Am J Hum Genet,2024

4. Adaptive long‐read sequencing reveals GGC repeat expansion in ZFHX3 associated with spinocerebellar ataxia type 4;Chen Z;Mov Disord,2024

5. Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs;Paucar M;medRxiv,2023

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