TY  - GEN
AU  - Hall,D A
AU  - Leehey,M A
AU  - Filley,C M
AU  - Steinbart,E
AU  - Montine,T
AU  - Schellenberg,G D
AU  - Bosque,P
AU  - Nixon,R
AU  - Bird,T
TI  - PRNP H187R mutation associated with neuropsychiatric disorders in childhood and dementia
SN  - 1526-632X
PY  - 2006///0210
KW  - Adolescent
KW  - Adult
KW  - Age of Onset
KW  - Brain
KW  - metabolism
KW  - Child
KW  - DNA Mutational Analysis
KW  - Dementia
KW  - complications
KW  - Disease Progression
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - genetics
KW  - Genetic Testing
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Mental Disorders
KW  - Middle Aged
KW  - Mutation
KW  - Neurons
KW  - Pedigree
KW  - Prion Diseases
KW  - Prions
N1  - Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1212/01.WNL.0000156911.70131.06
ER  -