Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy (Q36301666)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy |
scientific article |
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Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy (English)
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Emmanuel Mignot
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Juliette Faraco
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Ferdinando Cornelio
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Tim M Strom
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Francesca Poli
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Barbara Schormair
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Joachim Hallmayer
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Ling Lin
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Atle Melberg
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Alexander E Urban
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Fabian Grubert
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Thomas Wieland
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Elisabeth Graf
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9 February 2012
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2205-2210
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Identifiers
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