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).

Download

Full text not available from this repository.

Item Type: Article
Digital Object Identifier (DOI): doi:10.1038/ng.830
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
Accepted Date and Publication Date:
Status
1 May 2011Published
Date Deposited: 01 May 2012 13:53
Last Modified: 31 Mar 2016 14:27
URI: http://eprints.soton.ac.uk/id/eprint/337666

Actions (login required)

View Item View Item