Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosis. [electronic resource]
Producer: 20060207Description: 764-7 p. digitalISSN:- 0960-8966
- Adolescent
- Arginine -- genetics
- Charcot-Marie-Tooth Disease -- complications
- DNA Mutational Analysis -- methods
- DNA-Binding Proteins -- genetics
- Female
- Glutamine -- genetics
- Humans
- Male
- Mutation
- Neural Conduction -- physiology
- Neurologic Examination
- Peripheral Nerves -- physiopathology
- Radiography
- Scoliosis -- complications
- Trans-Activators -- genetics
- Transcriptional Regulator ERG
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Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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