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- 2024
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Mark
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4 : A poly-glycine disease
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- Contribution to journal › Article
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Mark
Clinical and genetic analyses of a Swedish patient series diagnosed with ataxia
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- Contribution to journal › Article
- 2020
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Mark
New generation genetic testing entering the clinic
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- Contribution to journal › Article
- 2017
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Mark
Ataxia-pancytopenia syndrome with SAMD9L mutations
(
- Contribution to journal › Article