A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype. [electronic resource]
Producer: 20090408Description: 1433-8 p. digitalISSN:- 1708-8283
- Adult
- Black or African American
- Arginine -- genetics
- Child
- Child, Preschool
- Chromosomes, Human, Pair 5
- DNA Mutational Analysis -- methods
- Family Health
- Female
- Humans
- Male
- Middle Aged
- Muscle Hypertonia -- genetics
- Mutation
- Phenotype
- Proline -- genetics
- Receptors, Glycine -- genetics
- Reflex, Abnormal -- genetics
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Publication Type: Journal Article
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