Identification of the Linkage of Mutations Causing Cystic Fibrosis to Different Alleles of a Tetranucleotide Repeat in Intron 6a of the CFTR Gene

Potapova O.Y., Voronina O.V., Gaitskhoki V.S., Bogacheva E.V., Uembitskaya T.E., Kuprina E.A., Kapranov N.I., Berlin Y.A., Schwartz E.I.
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Abstract

The linkage of the intragenic polymorphic (GATT)n repeat to a number of cystic fibrosis transmembrane conductance regulator gene mutations (delta F-508, G542X, G551D, R553X, R1162X, W1282X, N1303K, R334W, and R347P) was studied. The linkage of delta F-508, G542X, and N1303K to a six-copy allele and of R334W to a seven-copy allele of the repeat was found.
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导致囊性纤维化的突变与CFTR基因6a内含子四核苷酸重复序列不同等位基因连锁的鉴定
研究了基因内多态性(GATT)n重复序列与多个囊性纤维化跨膜传导调节基因突变(Δ F-508、G542X、G551D、R553X、R1162X、W1282X、N1303K、R334W和R347P)的连锁关系。发现Δ F-508、G542X和N1303K与重复序列的6拷贝等位基因连锁,R334W与重复序列的7拷贝等位基因连锁。
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