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.

Sun, Lin

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. [electronic resource] - Prion 2015 - 228-35 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1933-690X

10.1080/19336896.2015.1054601 doi


Base Sequence
Brain--pathology
Codon--genetics
Electroencephalography
Female
Homozygote
Humans
Insomnia, Fatal Familial--genetics
Magnetic Resonance Imaging
Male
Methionine--genetics
Middle Aged
Molecular Sequence Data
Mutation--genetics
Pedigree
Prions--genetics