An 8.5-kb segment of the PMP22 promoter
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Wayel Orfali; Robert N. Nicholson; Marie-Christine Guiot; Alan C. Peterson; G. J
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Article
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2005
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John Wiley and Sons
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English
⚖ 281 KB
Altered expression of the PMP22 gene causes Charcot-Marie-Tooth disease type 1A (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP). We have examined the promoter activity of 8.5 kb upstream of the first coding exon of the rat peripheral myelin protein-22 (rPmp22) gene in tra