Human mtDNA and Y-chromosome variation is correlated with matrilocal versus patrilocal residence |
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| Authors: | Oota H Settheetham-Ishida W Tiwawech D Ishida T Stoneking M |
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| Institution: | Division of Genetics and Development, Department of Pediatrics, University of Washington, Seattle, USA. |
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| Abstract: | IPEX is a fatal disorder characterized by immune dysregulation, polyendocrinopathy, enteropathy and X-linked inheritance (MIM 304930). We present genetic evidence that different mutations of the human gene FOXP3, the ortholog of the gene mutated in scurfy mice (Foxp3), causes IPEX syndrome. Recent linkage analysis studies mapped the gene mutated in IPEX to an interval of 17-20-cM at Xp11. 23-Xq13.3. |
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