CFTR MUTATIONS IN CHILEAN CYSTIC-FIBROSIS PATIENTS

被引:0
作者
RIOS, J
ORELLANA, O
ASPILLAGA, M
AVENDANO, I
LARGO, I
RIVEROS, N
机构
[1] HOSP NINOS LUIS CALVO MACKENNA, DEPT PEDIAT & BRONCOPULM, SANTIAGO 7, CHILE
[2] UNIV CHILE, FAC MED, DEPT BIOQUIM, SANTIAGO, CHILE
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中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
An analysis of five of the most common cystic fibrosis (CF) mutations worldwide (Delta F-508, R-553X, G-551D, N-1303K and G-542X) was performed in 36 Chilean patients. Polymerase chain reaction (PCR) amplification of the DNA followed by allele specific restriction enzyme analysis was used for detection. The overall frequencies of the mutations in the chromosomes analyzed were 29.2% for Delta F-508 and 4.2% for R-553X (n = 72). The G-542X, G-551D and N-1303 K mutations were absent in the Chilean sample. Our data suggest however that Delta F-508 is not the most common CF mutation in Chilean patients. Delta F-508 and R-553X account for only 33.4% of the alleles; 66.6% of them do not respond to the probes used and still remain uncharacterized.
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页码:291 / 294
页数:4
相关论文
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