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Detection of two point mutations causing familial defective apolipoprotein B-100 by heteroduplex analysis
Maritha J. Kotze, Elzet Langenhoven, Armand V. Peeters, Leonora Theart, C.J.Joubert OosthuizenVolume:
8
Year:
1994
Pages:
519
DOI:
10.1006/mcpr.1994.1072
File:
PDF, 329 KB
1994