TY  - GEN
AU  - Stamelou,Maria
AU  - Mencacci,Niccolo E
AU  - Cordivari,Carla
AU  - Batla,Amit
AU  - Wood,Nick W
AU  - Houlden,Henry
AU  - Hardy,John
AU  - Bhatia,Kailash P
TI  - Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiency
SN  - 1526-632X
PY  - 2012///1012
KW  - Adult
KW  - DNA Mutational Analysis
KW  - Dystonic Disorders
KW  - enzymology
KW  - Electroencephalography
KW  - Electromyography
KW  - Evoked Potentials, Somatosensory
KW  - genetics
KW  - Family Health
KW  - Female
KW  - Genotype
KW  - Humans
KW  - Male
KW  - Median Nerve
KW  - physiopathology
KW  - Point Mutation
KW  - Reflex
KW  - Tyrosine 3-Monooxygenase
KW  - deficiency
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1212/WNL.0b013e318261714a
ER  -