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cacna1g in Homo sapiens | Mus musculus | Rattus norvegicus | All 583 Gene records
See cacna1g in MedGen (2)
Spinocerebellar ataxia type 42
Spinocerebellar ataxia-42 (SCA42) is an autosomal dominant neurologic disorder characterized predominantly by gait instability and additional cerebellar signs such as dysarthria, nystagmus, and saccadic pursuits. The age at onset and severity of the disorder is highly variable. The disorder is slowly progressive (Coutelier et al., 2015). For a general discussion of autosomal dominant spinocerebellar ataxia, see SCA1 (164400). [from OMIM]
Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits
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