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Article

A Novel Compound Heterozygous Mutation in Aprataxin Causes Slowly Progressive Ataxia without Oculomotor Apraxia.

Movement disorders clinical practice - 1 Sept 2024

Satolli Sara, De Micco Rosa, Galatolo Daniele, Tessa Alessandra, Cirillo Mario, Tessitore Alessandro, Santorelli Filippo Maria

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PMID: 38881152
DOI: 10.1002/mdc3.14132
PMCID: PMC11452783

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