Article
Exclusion of malignant hyperthermia susceptibility (MHS) from a putative MHS2 locus on chromosome 17q and of the alpha 1, beta 1, and gamma subunits of the dihydropyridine receptor calcium channel as candidates for the molecular defect.
Human molecular genetics - 1 Jul 1993
Sudbrak R, Golla A, Hogan K, Powers P, Gregg R, Du Chesne I, Lehmann-Horn F, Deufel T
Abstract excerpt
Malignant hyperthermia (MH) is a potentially lethal pharmacogenetic disease with autosomal dominant inheritance triggered by exposure to commonly used inhalational anaesthetics or depolarising muscle relaxants. A MHS locus has been identified on human chromosome 19q12-q13.2 and the gene for the s...
Topics
- Alleles
- Base Sequence
- Calcium Channels
- Calcium Channels, L-Type
- Chromosome Mapping
- Chromosomes, Human, Pair 17
- DNA
- Female
- Genetic Markers
- Humans
- Male
- Malignant Hyperthermia
- Molecular Sequence Data
- Muscle Proteins