Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiency. [electronic resource]
Producer: 20121012Description: 435-41 p. digitalISSN:- 1526-632X
- 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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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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