Literature DB >> 1997213

Detection of mitochondrial DNA deletions in blood using the polymerase chain reaction: non-invasive diagnosis of mitochondrial myopathy.

J Poulton1, M E Deadman, D M Turnbull, B Lake, R M Gardiner.   

Abstract

Southern hybridisation demonstrates deleted mitochondrial DNAs (mtDNAs) in muscle but not in blood in a subgroup of patients with mitochondrial myopathy. The polymerase chain reaction (PCR) was used to search for low levels of rearranged mitochondrial DNAs in blood in 24 patients with mitochondrial myopathy, and 15 asymptomatic relatives, all of whom have no detectable abnormality on restriction enzyme analysis of blood mitochondrial DNA. In eight patients and two of their relatives, PCR products were obtained consistent with deletions of mitochondrial DNA. The presence or absence of a deletion was correctly predicted in 10 out of 11 patients from whom information was available from muscle DNA. No false positives were obtained in 43 controls. PCR analysis of blood may be applicable as a non-invasive screening test of affected individuals and in carrier detection.

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Year:  1991        PMID: 1997213     DOI: 10.1111/j.1399-0004.1991.tb02982.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  1 in total

1.  Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy.

Authors:  J Poulton; M E Deadman; J Bronte-Stewart; W S Foulds; R M Gardiner
Journal:  J Med Genet       Date:  1991-11       Impact factor: 6.318

  1 in total

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