Please use this identifier to cite or link to this item:
Scopus Web of Science® Altmetric
Type: Journal article
Title: Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation
Author: Lossi, A.
Laugier-Anfossi, F.
Depetris, D.
Gecz, J.
Gedeon, A.
Kooy, F.
Schwartz, C.
Mattei, M.
Croquette, M.
Villard, L.
Citation: Journal of Medical Genetics, 2002; 39(2):113-117
Publisher: British Med Journal Publ Group
Issue Date: 2002
ISSN: 0022-2593
Statement of
A-M Lossi, F Laugier-Anfossi, D Depetris, J Gecz, A Gedeon, F Kooy, C Schwartz, M-G Mattei, M-F Croquette, L Villard
Abstract: Non-syndromic X linked mental retardation (MRX) is a heterogeneous group of conditions in which all patients have mental retardation as the only constant phenotypic feature. We have identified a female patient with mental retardation and a balanced translocation involving chromosomes X and 21, t(X;21)(p11.2;q22.3). Physical mapping of the translocation breakpoint on the human X chromosome was performed using fluorescence in situ hybridisation. We have mapped the X chromosome breakpoint to a 21 kb DNA fragment upstream of the first exon of the KLF8 (ZNF741) gene in Xp11.21. We have subsequently shown that the KLF8 transcript is no longer detected in cells from the patient, although KLF8 expression is otherwise normally present in control lymphoblasts. Mutation screening of probands from 20 unrelated XLMR families linked to the proximal short arm of the human X chromosome failed to show any mutation in the coding region of the KLF8 gene.
Keywords: X linked mental retardation
Description: Copyright © 2002 by the BMJ Publishing Group Ltd.
DOI: 10.1136/jmg.39.2.113
Published version:
Appears in Collections:Aurora harvest
Paediatrics publications

Files in This Item:
File Description SizeFormat 
hdl_7523.pdf179.63 kBPublisher's PDF View/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.