Skip to main navigation Skip to search Skip to main content

Submikroskopiske kromosomanomalier som årsag til skizofreni

Translated title of the contribution: Submicroscopic chromosomal anomalies as a cause of schizophrenia

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.
Translated title of the contributionSubmicroscopic chromosomal anomalies as a cause of schizophrenia
Original languageDanish
JournalUgeskrift for Laeger
Volume170
Issue number46
Pages (from-to)3773-6
Number of pages4
ISSN0041-5782
Publication statusPublished - 2008

Fingerprint

Dive into the research topics of 'Submicroscopic chromosomal anomalies as a cause of schizophrenia'. Together they form a unique fingerprint.

Cite this