Spinocerebellar ataxia type 35 in California

1 specialist · 5 treatment centers for Spinocerebellar ataxia type 35 in California, verified against ClinicalTrials.gov, PubMed, and the NPPES NPI registry.

Spinocerebellar ataxia type 35 (SCA35) is a rare, inherited neurodegenerative disorder caused by mutations in the TGM6 gene, which encodes transglutaminase 6. This enzyme is predominantly expressed in the brain, particularly in the cerebellum, and plays a role in protein cross-linking…

Specialists are identified from ClinicalTrials.gov principal investigators, PubMed publications, and the NPI registry, then ranked through an automated scoring pipeline.
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Spinocerebellar ataxia type 35 care in other states

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