ID
45019
Beschrijving
Principal Investigator: Jerry Kim, MD, Department of Anesthesiology and Pain Medicine, University of Washington School of Medicine, Seattle, WA, USA MeSH: Malignant Hyperthermia https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000405 Malignant hyperthermia (MH) is a genetic disorder that causes a profound metabolic derangement following exposure to certain anesthetics. While approximately half of all cases are associated with ryanodine receptor-1 gene (RYR1) mutations, many cases have an unknown genetic cause. We sought to identify rare variants in novel MH candidate genes by sequencing the protein-coding regions of the genomes of individuals whose disease was either ruled in or out by the gold-standard diagnostic test. We also carefully selected individuals from well-characterized families to use gene-sharing information and maximize efficiency in the study design. Exome sequencing has helped identify the causes of over a dozen Mendelian disorders, has high power at low sample sizes, and is cost-efficient compared to whole-genome sequencing.
Link
https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000405
Trefwoorden
Versies (2)
- 13-07-22 13-07-22 - Dr. Christian Niklas
- 12-10-22 12-10-22 - Adrian Schulz
Houder van rechten
Jerry Kim, MD, Department of Anesthesiology and Pain Medicine, University of Washington School of Medicine, Seattle, WA, USA
Geüploaded op
13 juli 2022
DOI
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Licentie
Creative Commons BY 4.0
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dbGaP phs000405 Next Generation Mendelian Genetics: Malignant Hyperthermia
Eligibility Criteria
- StudyEvent: SEV1
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Eligibility Criteria
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