Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy

Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy is a paper indexed in ScholarIQ from OpenAlex.

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Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy has 265 citations in the OpenAlex counts ScholarIQ stores.

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Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy has 2012 year in the ScholarIQ index.

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Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy has bronze oa status in the ScholarIQ index.

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