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; Dyck, Peter J

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; Dyck, Peter J.

Affiliation

Klein CJ; Mayo Clinic, Department of Neurology, Division of Peripheral Nerve Diseases, Rochester, Minnesota, USA. klein.christopher@mayo.edu

Nat Genet ; 43(6): 595-600, 2011 Jun.

Article de En | MEDLINE | ID: mdl-21532572

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: DNA (cytosine-5-)-methyltransferase Limites: Adolescent / Adult / Female / Humans / Male / Middle aged Langue: En Journal: Nat Genet Sujet du journal: GENETICA MEDICA Année: 2011 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: États-Unis d'Amérique

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