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Publication Detail
Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome (vol 95, pg 611, 2014)
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Publication Type:Journal article
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Publication Sub Type:Correction
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Authors:Thomas AC, Williams H, Seto-Salvia N, Bacchelli C, Jenkins D, O'Sullivan M, Mengrelis K, Ishida M, Ocaka L, Chanudet E, James C, Lescai F, Anderson G, Morrogh D, Ryten M, Duncan AJ, Pai YJ, Saraiva JM, Ramos F, Farren B, Saunders D, Vernay B, Gissen P, Straatmaan-Iwanowska A, Baas F, Wood NW, Hersheson J, Houlden H, Hurst J, Scott R, Bitner-Glindzicz M, Moore GE, Sousa SB, Stanier P
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Publisher:CELL PRESS
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Publication date:04/06/2015
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Pagination:1008, 1009
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Journal:AMERICAN JOURNAL OF HUMAN GENETICS
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Volume:96
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Issue:6
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Status:Published
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Print ISSN:0002-9297
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Language:English
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Keywords:Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity
Abstract
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