Nonspecific X-linked mental retardation is a heterogeneous condition consisting of nonsyndromal mental retardation in males. It is caused by mutation in one of several genes on the X chromosome (MRX genes). Here we report on the localization of a presumptive MRX gene to chromosomal region Xq24-q26 i
Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation
โ Scribed by Gedeon, A. K.; Glass, I. A.; Connor, J. M.; Mulley, J. C.
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 28 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0148-7299
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โฆ Synopsis
A large family with non-specific X-linked mental retardation (MRX) was first described in 1991 [Glass et al., 19911, with a suggestion of linkage to Xq26-27. The maximum lod score was 1.60 (0 = 0.10) with the F9 locus. The localisation of this MRX gene has now been established by linkage to microsatellite markers. Peak pairwise lod scores of 4.02 and 4.01 (0 = 0.00) were attained at the D X S l l l 4 and DXS994 loci respectively. This MRX gene is now designated MRX27 and is localised to Xq24-26 by recombination events detected by DXS424 and DXS102. This regional localisation spans 26.2 cM on the genetic background map and defines another distinct MRX interval by linkage to a specific region of the X chromo-Some.
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