DOUBLE MUTANT ALLELES - ARE THEY RARE

被引:57
作者
SAVOV, A
ANGELICHEVA, D
BALASSOPOULOU, A
JORDANOVA, A
NOUSSIAARVANITAKIS, S
KALAYDJIEVA, L
机构
[1] UNIV SOFIA,HOSP OBSTET,MOLEC PATHOL LAB,BU-1431 SOFIA,BULGARIA
[2] LAIKON GEN HOSP,PRENATAL DIAG UNIT,GR-11526 ATHENS,GREECE
[3] AHEPA HOSP,DEPT PEDIAT 4,THESSALONIKI,GREECE
[4] EDITH COWAN UNIV,DEPT HUMAN BIOL,PERTH,WA 6027,AUSTRALIA
关键词
D O I
10.1093/hmg/4.7.1169
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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页码:1169 / 1171
页数:3
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