TY  - GEN
AU  - Baets,Jonathan
AU  - Duan,Xiaohui
AU  - Wu,Yanhong
AU  - Smith,Gordon
AU  - Seeley,William W
AU  - Mademan,Inès
AU  - McGrath,Nicole M
AU  - Beadell,Noah C
AU  - Khoury,Julie
AU  - Botuyan,Maria-Victoria
AU  - Mer,Georges
AU  - Worrell,Gregory A
AU  - Hojo,Kaori
AU  - DeLeon,Jessica
AU  - Laura,Matilde
AU  - Liu,Yo-Tsen
AU  - Senderek,Jan
AU  - Weis,Joachim
AU  - Van den Bergh,Peter
AU  - Merrill,Shana L
AU  - Reilly,Mary M
AU  - Houlden,Henry
AU  - Grossman,Murray
AU  - Scherer,Steven S
AU  - De Jonghe,Peter
AU  - Dyck,Peter J
AU  - Klein,Christopher J
TI  - Defects of mutant DNMT1 are linked to a spectrum of neurological disorders
SN  - 1460-2156
PY  - 2015///0616
KW  - Adult
KW  - Aged
KW  - Autophagy
KW  - genetics
KW  - DNA (Cytosine-5-)-Methyltransferase 1
KW  - DNA (Cytosine-5-)-Methyltransferases
KW  - chemistry
KW  - Female
KW  - HEK293 Cells
KW  - Hereditary Sensory and Autonomic Neuropathies
KW  - diagnosis
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Mutation
KW  - Nervous System Diseases
KW  - Pedigree
KW  - Protein Structure, Secondary
N1  - Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1093/brain/awv010
ER  -