L. Soria

Association between a specific apo B mutation and familial defective apoB100

L. Soria, 1989 .

Familial defective apo B‐100, characterization of an Italian family

A. Catapano, A. Corsini, R. Fumagalli, 1991, European journal of clinical investigation.

A polymorphism in a region with enhancer activity in the second intron of the human apolipoprotein B gene.

B. Mccarthy, B. Levy-Wilson, B. Blackhart, 1991, Journal of lipid research.

Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100.

S. Grundy, G. Vega, H. R. Clarke, 1989, Proceedings of the National Academy of Sciences of the United States of America.