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), 595-600. (doi:10.1038/ng.830).

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Item Type: Article
ISSNs: 1061-4036 (print)
1546-1718 (electronic)
Related URLs:
Subjects: Q Science > QH Natural history > QH426 Genetics
Divisions: Faculty of Medicine > Human Development and Health
ePrint ID: 337666
Date Deposited: 01 May 2012 13:53
Last Modified: 27 Mar 2014 20:21
URI: http://eprints.soton.ac.uk/id/eprint/337666

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