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Faculty Opinions recommendation of Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy. — Manel Esteller | RDL Network
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Faculty Opinions recommendation of Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy.
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Manel Esteller
University of Barcelona
Faculty Opinions recommendation of Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy.
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Manel Esteller
University of Barcelona
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