A newly identified null allelic mutation in the human lipoprotein lipase (LPL) gene of a compound heterozygote with familial LPL deficiency
- 14 April 1992
- journal article
- research article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Vol. 1138 (4) , 353-356
- https://doi.org/10.1016/0925-4439(92)90015-f
Abstract
No abstract availableKeywords
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