T. M. Narcisi

Characterization of genetic markers in the 5′ flanking region of the apo A1 gene

J. Scott, C. Shoulders, A. Jarmuz, 1993, Human Genetics.

VNTR polymorphism in the hepatic lipase gene (LIPC).

P. Cullen, J. Scott, M. Schotz, 1991, Nucleic Acids Research.

Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein.

P. Cullen, C. Shoulders, R. Pease, 1993, Human molecular genetics.

Mutations of the microsomal triglyceride-transfer-protein gene in abetalipoproteinemia.

M. Fox, S. Povey, C. Shoulders, 1995, American journal of human genetics.

The abetalipoproteinemia gene is a member of the vitellogenin family and encodes an α–helical domain

D. Levitt, L. Banaszak, C. Shoulders, 1994, Nature Structural Biology.

Dinucleotide repeat polymorphisms at the lipoprotein lipase (LPL) locus

J. Scott, C. Shoulders, M. Schotz, 1993, Human Genetics.