TY  - GEN
AU  - Li,Jun
AU  - Ghandour,Khaled
AU  - Radovanovic,Danijela
AU  - Radovanovic,Danuijola
AU  - Shy,Rosemary R
AU  - Krajewski,Karen M
AU  - Shy,Michael E
AU  - Nicholson,Garth A
TI  - Stoichiometric alteration of PMP22 protein determines the phenotype of hereditary neuropathy with liability to pressure palsies
SN  - 0003-9942
PY  - 2007///0831
KW  - Adolescent
KW  - Adult
KW  - Aged
KW  - Aged, 80 and over
KW  - Child
KW  - DNA Mutational Analysis
KW  - Down-Regulation
KW  - genetics
KW  - Electrodiagnosis
KW  - Female
KW  - Frameshift Mutation
KW  - Genetic Markers
KW  - Genetic Predisposition to Disease
KW  - Genetic Testing
KW  - Heredodegenerative Disorders, Nervous System
KW  - Humans
KW  - Leucine
KW  - Male
KW  - Middle Aged
KW  - Myelin Proteins
KW  - biosynthesis
KW  - Neural Conduction
KW  - Peripheral Nerves
KW  - metabolism
KW  - Peripheral Nervous System Diseases
KW  - Phenotype
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1001/archneur.64.7.974
ER  -