Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome (Q34478269)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome |
scientific article |
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Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome (English)
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Mina Ryten
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Maria Bitner-Glindzicz
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Anna C Thomas
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Hywel Williams
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Núria Setó-Salvia
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Chiara Bacchelli
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Dagan Jenkins
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Konstantinos Mengrelis
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Miho Ishida
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Louise Ocaka
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Estelle Chanudet
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Chela James
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Francesco Lescai
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Glenn Anderson
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Deborah Morrogh
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Andrew J Duncan
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Yun Jin Pai
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Jorge M Saraiva
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Fabiana Ramos
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Bernadette Farren
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Dawn Saunders
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Anna Straatmaan-Iwanowska
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Joshua Hersheson
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Henry Houlden
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Jane Hurst
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Richard Scott
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Gudrun E Moore
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Sérgio B Sousa
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6 November 2014
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Identifiers
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