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. 2011 Jun;52(6):1162–1169. doi: 10.1194/jlr.M011155

Fig. 4.

Fig. 4.

LMF1 deficiency abrogates plasma phospholipase activity. Heparin-released salt-sensitive phospholipase activity in a patient carrying the homozygous LMF1W464X mutation (closed symbol) is expressed as a percentage of mean of control subjects (open symbols).