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Double mutant alleles: are they rare?

作者信息

Savov A, Angelicheva D, Balassopoulou A, Jordanova A, Noussia-Arvanitakis S, Kalaydjieva L

机构信息

Laboratory of Molecular Pathology, University Hospital of Obstetrics, Sofia, Bulgaria.

出版信息

Hum Mol Genet. 1995 Jul;4(7):1169-71. doi: 10.1093/hmg/4.7.1169.

Abstract

The presence of two different mutations carried by the same CF allele has been demonstrated in four out of 44 Bulgarian CF patients during a systematic search of the entire coding sequence of the CFTR gene. Two of the double mutant alleles include one nonsense and one missense mutation and although the nonsense mutation can be considered to be the main defect, the amino acid substitutions are good candidates for disease-causing mutations as well. One double mutant carries two missense mutations whose contribution to the CF phenotype is difficult to evaluate. The findings suggest that double mutant alleles may be more common than expected and could account for some of the problems in phenotype-genotype correlations. Such alleles may have important implications for molecular diagnosis and genetic counselling.

摘要

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