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Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss

Klein, Christopher J., Botuyan, Maria-Victoria, Wu, Yanhong, Ward, Christopher J., Nicholson, Garth A., Hammans, Simon, Hojo, Kaori, Yamanishi, Hiromitch, Karpf, Adam R., Wallace, Douglas C., Simon, Mariella, Lander, Cecilie, Boardman, Lisa A., Cunningham, Julie M., Smith, Glenn E., Litchy, William J., Boes, Benjamin, Atkinson, Elizabeth J., Middha, Sumit, B Dyck, P. James, Parisi, Joseph E., Mer, Georges, Smith, David I. and Dyck, Peter J. (2011) Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss Nature Genetics, 43, (6), pp. 595-600. (doi:10.1038/ng.830).

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Published date: 1 May 2011
Organisations: Human Development & Health


Local EPrints ID: 337666
ISSN: 1061-4036
PURE UUID: 374f90b6-e554-40d9-be32-7102c276f2e5

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Date deposited: 01 May 2012 13:53
Last modified: 18 Jul 2017 06:01

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Author: Christopher J. Klein
Author: Maria-Victoria Botuyan
Author: Yanhong Wu
Author: Christopher J. Ward
Author: Garth A. Nicholson
Author: Simon Hammans
Author: Kaori Hojo
Author: Hiromitch Yamanishi
Author: Adam R. Karpf
Author: Douglas C. Wallace
Author: Mariella Simon
Author: Cecilie Lander
Author: Lisa A. Boardman
Author: Julie M. Cunningham
Author: Glenn E. Smith
Author: William J. Litchy
Author: Benjamin Boes
Author: Elizabeth J. Atkinson
Author: Sumit Middha
Author: P. James B Dyck
Author: Joseph E. Parisi
Author: Georges Mer
Author: David I. Smith
Author: Peter J. Dyck

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