Fig. 1
From: Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia
Patients of the Algerian cohort with identified forms of ARCA. AOA1, Ataxia with oculomotor aparaxia type 1; AOA2, Ataxia with oculomotor aparaxia type 2; ARSACS, Autosomal recessive spastic ataxia of Cherlevoix-Saguenay; AVED, Ataxia with isolated vitamin E deficiency; FRDA, Friedreich ataxia; MSS, Marinesco-Sjögren syndrome; PHARC, Polyneupathy, hearing loss, ataxia, retinitis pigmentosa and cataract; SCAR8, Spinocerebellar ataxia, autosomal recessive 8 (or ARCA1); SCAR9, Spinocerebellar ataxia, autosomal recessive 9 (or ARCA2)