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

Klein, Christopher J

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss. [electronic resource] - Nature genetics Jun 2011 - 595-600 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

1546-1718

10.1038/ng.830 doi


Adolescent
Adult
DNA (Cytosine-5-)-Methyltransferase 1
DNA (Cytosine-5-)-Methyltransferases--genetics
DNA Methylation
Dementia--genetics
Female
G2 Phase
Hearing Loss--genetics
Hereditary Sensory and Autonomic Neuropathies--genetics
Heterochromatin--metabolism
Humans
Male
Middle Aged
Models, Molecular
Mutation