Pediatric Neurology
 2024
DOI: 10.1016/j.pediatrneurol.2024.12.011
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Genetic homogeneity of a TDP1 variant, c.1478A>G, as the main disease-causing variant of Spinocerebellar ataxia with axonal neuropathy 1 (SCAN1) in Middle East and a Systematic Review

Mahsa Mohammadi,
Moez Ravanbod,
Aida Ghasemi
et al.
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