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W13.321 Compound heterozygosity for a known (G188E) and novel (W394X) LPL gene mutation causing familial lipoprotein lipase deficiency

✍ Scribed by Crawford, G.; Wats, G.F.; Robertson, K.; Burnett, J.R.; van Bockxmeer, F.

Book ID: 118632715
Publisher: Elsevier Science
Year: 2004
Tongue: English
Weight: 152 KB
Volume: 5
Category: Article
ISSN: 1567-5688
DOI: 10.1016/s1567-5688(04)90320-6

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