Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family.

Nonspecific X-linked mental retardation is a nonprogressive, genetically heterogeneous condition that affects cognitive function in the absence of other distinctive clinical manifestations. We report here linkage data on a large Pakistani family affected by a form of X-linked nonspecific mental retardation. X chromosome genotyping of family members and linkage analysis allowed the identification of a new disease locus, MRX53. The defined critical region spans approximately 15 cM between DXS1210 and DXS1047 in Xq22.2-26. A LOD score value of 3.34 at no recombination was obtained with markers DXS1072 and DXS8081.

[1]  C. Walsh,et al.  Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation. , 2000, American journal of medical genetics.

[2]  J. Gécz,et al.  Genes for cognitive function: developments on the X. , 2000, Genome research.

[3]  A. Meindl,et al.  A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation , 2000, Nature Genetics.

[4]  J Liu,et al.  Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardation. , 1999, Genomics.

[5]  R. Stevenson,et al.  Molecular cloning and characterization of TRPC5 (HTRP5), the human homologue of a mouse brain receptor-activated capacitative Ca2+ entry channel. , 1999, Genomics.

[6]  Lin Jun,et al.  A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation , 1999, Nature Genetics.

[7]  J. Gécz,et al.  A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation , 1999, Nature Genetics.

[8]  H. Lubs,et al.  XLMR genes: update 1998. , 1999, American journal of medical genetics.

[9]  C. Walsh,et al.  PAK3 mutation in nonsyndromic X-linked mental retardation , 1998, Nature Genetics.

[10]  Andrea Menegon,et al.  Mutations in GDI1 are responsible for X-linked non-specific mental retardation , 1998, Nature Genetics.

[11]  H. R. Crollius,et al.  Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation , 1998, Nature.

[12]  I. Scheffer,et al.  doublecortin , a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein , 1998, Cell.

[13]  Y. Berwald‐Netter,et al.  A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome , 1998, Cell.

[14]  K. Dry,et al.  Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3. , 1996, Genomics.

[15]  A. Donnelly,et al.  How many X-linked genes for non-specific mental retardation (MRX) are there? , 1996, American journal of medical genetics.

[16]  J. Gécz,et al.  Identification of the gene FMR2, associated with FRAXE mental retardation , 1996, Nature Genetics.

[17]  R. Gibbs,et al.  Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island , 1996, Nature Genetics.

[18]  P. Marynen,et al.  Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35). , 1996, Journal of medical genetics.

[19]  H. Lubs,et al.  XLMR genes: update 1990. , 1991, American journal of medical genetics.

[20]  J. Ott,et al.  Strategies for multilocus linkage analysis in humans. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[21]  J. Chelly Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation. , 1999, Human molecular genetics.