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- W2368136987 abstract "Aim: To detect the deletion of the Parkin gene in a Chinese pedigree with autosomal Parkinson′s disease. Methods: A total of 14 pairs of primers designed from exon and intron sequences of the Parkin gene were used for the amplification. PCR was carried out with human genomic DNA as the template. The PCR products were sequenced after being purified. Deletion was identified by comparing DNA sequences of the patients in a Chinese pedigree with that of normal control. Results: The deletion of 110 base pairs was detected in exon 3 of the Parkin gene in the detected pedigree. The variation of some base pairs on the exon 4 and exon 5 was also detected. Conclusion: The deletion in exon 3 of Parkin gene is useful for the early diagnosis and gene therapy of the disease." @default.
- W2368136987 created "2016-06-24" @default.
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- W2368136987 date "2006-01-01" @default.
- W2368136987 modified "2023-09-24" @default.
- W2368136987 title "Sequencing analysis on gene deletion causing autosomal Parkinson′s disease in a Chinese pedigree" @default.
- W2368136987 hasPublicationYear "2006" @default.
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