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Technical Briefs |
1 Department of Chemical Pathology, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China;2 Division of Clinical Biochemistry, Queen Mary Hospital, Hong Kong, China;
aaddress correspondence to this author at: Department of Chemical Pathology, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China; fax 852-26365090, e-mail ching-wanlam{at}cuhk.edu.hk
Abstract
Background: We investigated the mechanisms leading to allele dropoutthe nonamplification of 1 of the allelesin PCR-based diagnosis of Wilson disease (WD).
Methods: We extracted genomic DNA from blood samples from 6 WD patients (P1P6) with allele dropouts detected in a previous study of WD in a Hong Kong Chinese population. We amplified the ATP7B gene by PCR and performed direct DNA sequencing of all exons of the ATP7B gene. To support the proposed mechanism of allele dropout, we used proofreading DNA polymerase, primer design avoiding single-nucleotide polymorphism sites, and duplex PCR.
Results: Patients P1P4 were all apparently homozygous for a known disease-causing mutation, c.2975C>T (p.P992L) in exon 13. Patient P5 was apparently homozygous for a novel mutation, c.2524G>A, and patient P6 was apparently homozygous for another known mutation, c.522_523insA (p.K175K-fs). In all cases, we determined that the patients were actually heterozygous for these mutations.
Conclusion: Our results confirm that allele dropout is the mechanism causing apparent homozygosity of heterozygous mutations in these WD patients.
The following articles in journals at HighWire Press have cited this article:
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C. M. Mak, C.-W. Lam, and S. Tam Diagnostic Accuracy of Serum Ceruloplasmin in Wilson Disease: Determination of Sensitivity and Specificity by ROC Curve Analysis among ATP7B-Genotyped Subjects Clin. Chem., August 1, 2008; 54(8): 1356 - 1362. [Abstract] [Full Text] [PDF] |
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A. Gupta, P. Nasipuri, S. K. Das, and K. Ray Simple and Effective Strategies for Detection of Allele Dropout in PCR-Based Diagnosis of Wilson Disease. Clin. Chem., August 1, 2006; 52(8): 1611 - 1612. [Full Text] [PDF] |
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