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Medium-chain acyl-CoA dehydrogenase deficiency is not a cause of previously diagnosed Reye syndrome

✍ Scribed by C. A. Rupar; T. W. Frewen; B. A. Gordon


Publisher
Springer
Year
1995
Tongue
English
Weight
139 KB
Volume
18
Category
Article
ISSN
0141-8955

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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