Literature DB >> 10398244

Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1.

S Claes1, P Volcke, K Devriendt, M Holvoet, P Raeymaekers, J J Cassiman, J P Fryns.   

Abstract

Two families with nonspecific X-linked mental retardation (MRX) are presented. In the first family, MRX51, three male patients showed mild to borderline mental retardation. Multipoint linkage analysis yielded a maximal LOD score of 2.10 between markers DXS8012 and DXS1003, localizing the MRX51 gene at Xp11.3-p11.23. In the second family, XLMR7, three men showed moderate mental retardation (MR), and one possible female carrier had mild MR. Multipoint linkage analysis yielded an LOD score of 1.80 between markers DXS8063 and DXS1047, situating the disease gene at Xq23-q26.1. When the analysis was performed considering the affected female to be an expressing heterozygote carrier of the disease mutation, a maximal LOD score of 2.10 was found in the same region. Copyright 1999 Wiley-Liss, Inc.

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Year:  1999        PMID: 10398244

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

1.  UBE2A, which encodes a ubiquitin-conjugating enzyme, is mutated in a novel X-linked mental retardation syndrome.

Authors:  Rafaella M P Nascimento; Paulo A Otto; Arjan P M de Brouwer; Angela M Vianna-Morgante
Journal:  Am J Hum Genet       Date:  2006-07-03       Impact factor: 11.025

2.  The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability.

Authors:  Joke Vandewalle; Marijke Bauters; Hilde Van Esch; Stefanie Belet; Jelle Verbeeck; Nathalie Fieremans; Maureen Holvoet; Jodie Vento; Ana Spreiz; Dieter Kotzot; Edda Haberlandt; Jill Rosenfeld; Joris Andrieux; Bruno Delobel; Marie-Bertille Dehouck; Koen Devriendt; Jean-Pierre Fryns; Peter Marynen; Amy Goldstein; Guy Froyen
Journal:  Hum Genet       Date:  2013-06-20       Impact factor: 4.132

3.  Mapping the landscape of tandem repeat variability by targeted long read single molecule sequencing in familial X-linked intellectual disability.

Authors:  Alena Zablotskaya; Hilde Van Esch; Kevin J Verstrepen; Guy Froyen; Joris R Vermeesch
Journal:  BMC Med Genomics       Date:  2018-12-19       Impact factor: 3.063

  3 in total

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