TY  - GEN
AU  - Sun,Lin
AU  - Li,Xia
AU  - Lin,Xiang
AU  - Yan,Feng
AU  - Chen,Kathryn
AU  - Xiao,Shifu
TI  - Familial fatal insomnia with atypical clinical features in a patient with D178N mutation and homozygosity for Met at codon 129 of the prion protein gene
SN  - 1933-690X
PY  - 2016///0328
KW  - Base Sequence
KW  - Brain
KW  - pathology
KW  - Codon
KW  - genetics
KW  - Electroencephalography
KW  - Female
KW  - Homozygote
KW  - Humans
KW  - Insomnia, Fatal Familial
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Methionine
KW  - Middle Aged
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Pedigree
KW  - Prions
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1080/19336896.2015.1054601
ER  -