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Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiency.

Stamelou, Maria

Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiency. [electronic resource] - Neurology Jul 2012 - 435-41 p. digital

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

ISSN: 1526-632X

Standard No.: 10.1212/WNL.0b013e318261714a doi

Subjects--Topical Terms:
Adult
DNA Mutational Analysis
Dystonic Disorders--enzymology
Electroencephalography
Electromyography
Evoked Potentials, Somatosensory--genetics
Family Health
Female
Genotype
Humans
Male
Median Nerve--physiopathology
Point Mutation--genetics
Reflex--genetics
Tyrosine 3-Monooxygenase--deficiency
Young Adult

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