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Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia

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Academic year: 2021

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Table 1 Clinical features of a group of Algerian patients with autosomal recessive ataxia
Table 3 summarizes the molecular findings for the patients/families for which the mutations were identified.
Table 4 Genotype/phenotype correlations in a group of patients of the Algerian cohort FRDA (26P/18 F) AVED (12P/10 F) AOA2 (6P/6 F) ARSACS(8P/6 F) AOA1 (2P/2 F) SACR9 (5P/3 F) PHARC (2P/1 F) SCAR8 (1P/1 F) MSS (1P/1 F) Age at onset (range) 12.74 ± 7.15
Fig. 1 Patients of the Algerian cohort with identified forms of ARCA.

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