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Molecular basis of inherited medium-chain acyl-CoA dehydrogenase deficiency causing sudden child death

✍ Scribed by D. P. Kelly; D. E. Hale; S. L. Rutledge; M. L. Ogden; A. J. Whelan; Z. Zhang; A. W. Strauss


Publisher
Springer
Year
1992
Tongue
English
Weight
831 KB
Volume
15
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