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Illegitimate transcription of phenylalanine hydroxylase for detection of mutations in patients with phenylketonuria.

作者信息

Ramus S J, Forrest S M, Cotton R G

机构信息

Olive Miller Protein Laboratory, Murdoch Institute, Royal Childrens Hospital, Melbourne, Victoria, Australia.

出版信息

Hum Mutat. 1992;1(2):154-8. doi: 10.1002/humu.1380010211.

DOI:10.1002/humu.1380010211
PMID:1301202
Abstract

Illegitimately transcribed phenylalanine hydroxylase mRNA was amplified using the polymerase chain reaction from both fibroblasts and Epstein-Barr virus-transformed lymphocytes. This method was used to study mutations of this gene in patients with phenylketonuria and known point mutations were easily detected. Illegitimate transcription was successful for studying splicing defects and it was found that the previously described mutation which changes G to A at the 5' donor site of intron 7 causes exon 7 to be spliced out.

摘要

相似文献

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Rapid single-base mismatch detection in genotyping for phenylketonuria.苯丙酮尿症基因分型中的快速单碱基错配检测
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