A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus

BACKGROUND: Premature ovarian failure (POF) is characterized by elevated gonadotrophins and amenorrhea before the age of 40 years and occurs approximately in 1% of women. POF etiology is highly heterogeneous with a wide spectrum of etiological pathogenic mechanisms including genetic causes. These mostly involve numerical, structural or monogenic defects on the X-chromosome. Mutations in a small number of autosomal genes (such as FOXL2 and NOBOX) have been identified as a cause of POF. However, in most cases, the disease underlying mechanisms are largely unknown. METHODS: We performed a genome-... Mehr ...

Verfasser: Oldenburg, R.A. (Rogier)
Dooren, M.F. (Marieke) van
Graaf, B.M. (Bianca) de
Simons, E.J. (Erik)
Govaerts, L.C. (Lutgarde)
Swagemakers, S.M.A. (Sigrid)
Verkerk, A.J.H.M. (Annemieke)
Oostra, B.A. (Ben)
Bertoli Avella, A.M. (Aida)
Dokumenttyp: Artikel
Erscheinungsdatum: 2008
Schlagwörter: Familial / Genome-wide search / Linkage analysis / Premature ovarian failure / SNPs
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26677681
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : http://repub.eur.nl/pub/29501