Literature DB >> 8288232

Localization of a gene responsible for nonspecific mental retardation (MRX9) to the pericentromeric region of the X chromosome.

P Willems1, L Vits, I Buntinx, P Raeymaekers, C Van Broeckhoven, B Ceulemans.   

Abstract

Nonspecific X-linked mental retardation (MRX) includes several distinct entities with mental retardation but without additional distinguishing features. The MRX family reported here has been classified previously as MRX9. In this study, we performed linkage analysis of MRX9 with a panel of 43 polymorphic DNA markers dispersed over chromosome X. Two-point linkage analysis revealed lod scores of 3.52 and 3.82 at 0% recombination for OATL1 and MAOA, both located in Xp11.2-p11.4. Lod scores for linkage with PGK1P1, DXS106, and DXS132, all located in Xq11-q13, were 3.83, 3.82, and 3.52, respectively, all at 0% recombination. Multipoint linkage analysis showed two peaks with MAOA and DXS132/DXS106, respectively. Analysis of recombinational events indicated a position of the MRX9 gene between DXS164 and DXS453. These findings are compatible with a location of the MRX9 gene in the pericentromeric region of the X chromosome at Xp21-q13.

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Year:  1993        PMID: 8288232     DOI: 10.1006/geno.1993.1468

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  2 in total

Review 1.  The Emerging Field of Epitranscriptomics in Neurodevelopmental and Neuronal Disorders.

Authors:  Margarita T Angelova; Dilyana G Dimitrova; Nadja Dinges; Tina Lence; Lina Worpenberg; Clément Carré; Jean-Yves Roignant
Journal:  Front Bioeng Biotechnol       Date:  2018-04-13

Review 2.  RNA 2'-O-Methylation (Nm) Modification in Human Diseases.

Authors:  Dilyana G Dimitrova; Laure Teysset; Clément Carré
Journal:  Genes (Basel)       Date:  2019-02-05       Impact factor: 4.096

  2 in total

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