Spring til hovednavigation
Spring til søgning
Spring til hovedindhold
Københavns Universitets forskningsportal Forside
Hjælp og OSS
Dansk
English
Forside
Profiler
Publikation
Forskningsenheder
Presse/medier
Aktiviteter
Priser
???studenttheses???
Forskningsdatasæt
Søg efter ekspertise, navn eller tilknytning
The frequency of a disease-causing point mutation in the gene coding for medium-chain acyl-CoA dehydrogenase in sudden infant death syndrome
Jytte Banner
,
N Gregersen
, S Kølvraa, B Nørgaard Pedersen, M Gregersen, K Helweg-Larsen, J Simonsen
Afdeling for Retspatologi
TEO Afdeling for systematisk teologi
31
Citationer (Scopus)
Oversigt
Fingeraftryk
Fingeraftryk
Dyk ned i forskningsemnerne om 'The frequency of a disease-causing point mutation in the gene coding for medium-chain acyl-CoA dehydrogenase in sudden infant death syndrome'. Sammen danner de et unikt fingeraftryk.
Sorter
Vægt
Alfabetisk
Keyphrases
Gene Coding
100%
Point mutation
100%
Medium-chain acyl-CoA Dehydrogenase
100%
Sudden Infant Death Syndrome
100%
Cause of Disease
100%
Inherited Metabolic Diseases
50%
Etiology
25%
Polymerase Chain Reaction Assay
25%
Sudden Death
25%
Common Disease
25%
Dried Blood Spots
25%
Homozygosity
25%
Clinical Presentation
25%
Heterozygosity
25%
Underrepresentation
25%
Well-defined
25%
Biochemistry, Genetics and Molecular Biology
Medium-Chain Acyl-CoA Dehydrogenase
100%
Acyl-CoA
100%
Point Mutation
100%
Infancy
66%
Dried Blood Spot
33%
Polymerase Chain Reaction
33%
Homozygosity
33%
Heterozygosity
33%
Population
33%