Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis. [electronic resource]
Producer: 19950427Description: 44-7 p. digitalISSN:- 0022-2593
- Adolescent
- Adult
- Age of Onset
- Arginine -- genetics
- Base Sequence
- Calcium Channels -- genetics
- Calcium Channels, L-Type
- Child
- Chromosome Mapping
- Chromosomes, Human, Pair 1
- DNA Primers
- Female
- Genes, Dominant
- Genetic Linkage
- Histidine -- genetics
- Humans
- Hypokalemia -- genetics
- Male
- Molecular Sequence Data
- Muscle Proteins -- genetics
- Netherlands
- Paralyses, Familial Periodic -- blood
- Pedigree
- Point Mutation
- Receptors, Cholinergic -- genetics
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Publication Type: Journal Article
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