Submikroskopiske kromosomanomalier som årsag til skizofreni

Abstract

Although the inheritable nature of schizophrenia is well-established, the genetic underpinnings remain largely hidden. Recently, two independent research groups identified microdeletions conferring high risk of schizophrenia. The deletions are recurrent in nature and offer an explanation to the apparently stable prevalence of the disease, despite reduced fecundity in patients. The findings may lead to development of diagnostic tools and construction of new disease models to help the development of novel therapeutic strategies.
Bidragets oversatte titelSubmicroscopic chromosomal anomalies as a cause of schizophrenia
OriginalsprogDansk
TidsskriftUgeskrift for Laeger
Vol/bind170
Udgave nummer46
Sider (fra-til)3773-6
Antal sider4
ISSN0041-5782
StatusUdgivet - 2008

Emneord

  • Chromosome Deletion
  • Chromosomes, Human, Pair 1
  • Chromosomes, Human, Pair 15
  • Genetic Predisposition to Disease
  • Genome, Human
  • Humans
  • Schizophrenia

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