Functional characterization of mutations in inherited human cPLA₂ deficiency.

Reed KA, Tucker DE, Aloulou A, Adler D, Ghomashchi F, Gelb MH, Leslie CC, Oates JA, Boutaud O
Biochemistry. 2011 50 (10): 1731-8

PMID: 21247147 · PMCID: PMC3051024 · DOI:10.1021/bi101877n

MeSH Terms (10)

Animals Biocatalysis Cell Line Dogs Group IV Phospholipases A2 Humans Mice Mice, Knockout Mutation Protein Transport

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