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 PICO Portal from OpenAlex.

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

When was Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy published?

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

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

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