Institut for Biomedicin

Lars Bolund

The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the gene

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DOI

  • Steen Kølvraa
  • ,
  • Niels Gregersen
  • Alexandra I.F. Blakemore, University of Sheffield
  • ,
  • Anne K. Schneidermann, Aarhus Universitet
  • ,
  • Vibeke Winter, Aarhus Universitet
  • ,
  • Brage S. Andresen, Molecular Genetic Laboratory, Aarhus Universitet
  • ,
  • Diana Curtis, University of Sheffield
  • ,
  • Paul C. Engel, University of Sheffield
  • ,
  • Divry Pricille, Hopital Debrousse
  • ,
  • William Rhead, University of Iowa
  • ,
  • Lars Bolund

RFLP haplotypes in the region containing the medium-chain acyl-CoA dehydrogenase (MCAD) gene on chromosome 1 have been determined in patients with MCAD deficiency. The RFLPs were detected after digestion of patient DNA with the enzymes BanII, PstI and TaqI and with an MCAD cDNA-clone as a probe. Of 32 disease-causing alleles studied, 31 possesed the previously publised A→G point-mutation at position 985 of the cDNA. This mutation has been shown to result in inactivity of the MCAD enzyme. In at least 30 of the 31 alleles carrying this G985 mutation a specific RFLP haplotype was present. In contrast, the same haplotype was present in only 23% of normal alleles (P≤3.4×10-18). These findings are consistent with the existence of a pronounced founder effect, possibly combined with biological and/or sampling selection.

OriginalsprogEngelsk
TidsskriftHuman Genetics
Vol/bind87
Nummer4
Sider (fra-til)425-428
Antal sider4
ISSN0340-6717
DOI
StatusUdgivet - 1 aug. 1991

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