TY  - GEN
AU  - Klein,Christopher J
AU  - Botuyan,Maria-Victoria
AU  - Wu,Yanhong
AU  - Ward,Christopher J
AU  - Nicholson,Garth A
AU  - Hammans,Simon
AU  - Hojo,Kaori
AU  - Yamanishi,Hiromitch
AU  - Karpf,Adam R
AU  - Wallace,Douglas C
AU  - Simon,Mariella
AU  - Lander,Cecilie
AU  - Boardman,Lisa A
AU  - Cunningham,Julie M
AU  - Smith,Glenn E
AU  - Litchy,William J
AU  - Boes,Benjamin
AU  - Atkinson,Elizabeth J
AU  - Middha,Sumit
AU  - B Dyck,P James
AU  - Parisi,Joseph E
AU  - Mer,Georges
AU  - Smith,David I
AU  - Dyck,Peter J
TI  - Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss
SN  - 1546-1718
PY  - 2011///0726
KW  - Adolescent
KW  - Adult
KW  - DNA (Cytosine-5-)-Methyltransferase 1
KW  - DNA (Cytosine-5-)-Methyltransferases
KW  - genetics
KW  - DNA Methylation
KW  - Dementia
KW  - Female
KW  - G2 Phase
KW  - Hearing Loss
KW  - Hereditary Sensory and Autonomic Neuropathies
KW  - Heterochromatin
KW  - metabolism
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Models, Molecular
KW  - Mutation
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/ng.830
ER  -