Erratum: Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome (American Journal of Human Genetics (2014) 95 (611–621))

Thomas, A.C., Williams, H. ORCID: https://orcid.org/0000-0001-7758-0312, Seto-Salvia, S., 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, A.J., Pai, Y.J., Saraiva, J.M., Ramos, F., Farren, B., Saunders, D., Vernay, B., Gissen, P., Straatmaan-Iwanowska, A., Baas, F., Wood, N.W., Hersheson, J., Houlden, H., Hurst, J., Scott, R., Bitner-Glindzicz, M., Moore, G.E., Sousa, S.B. and Stanier, P. 2015. Erratum: Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome (American Journal of Human Genetics (2014) 95 (611–621)). American Journal of Human Genetics 96 (6) , pp. 1008-1009. 10.1016/j.ajhg.2015.05.010

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Item Type:	Article
Date Type:	Published Online
Status:	Published
Schools:	Medicine
Publisher:	Elsevier (Cell Press)
ISSN:	0002-9297
Last Modified:	26 Oct 2022 08:47
URI:	https://orca.cardiff.ac.uk/id/eprint/128312

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