Alternating Hemiplegia and Epilepsia Partialis Continua: A new phenotype for a novel compound TBC1D24 mutation. [electronic resource]
Producer: 20170417Description: 71-73 p. digitalISSN:- 1532-2688
- Brain -- physiopathology
- Carrier Proteins -- genetics
- Child, Preschool
- Diagnosis, Differential
- Electroencephalography
- Epilepsia Partialis Continua -- genetics
- Female
- GTPase-Activating Proteins
- Hemiplegia -- genetics
- High-Throughput Nucleotide Sequencing
- Humans
- Membrane Proteins
- Mutation
- Nerve Tissue Proteins
- Phenotype
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Publication Type: Case Reports; Journal Article
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