Young, S. G., Hubl, S. T., Smith, R. S., Snyder, S. M., & Terdiman, J. F. (1990). Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins.

Young, S G., S T. Hubl, R S. Smith, S M. Snyder, and J F. Terdiman. Familial Hypobetalipoproteinemia Caused By a Mutation in the Apolipoprotein B Gene That Results in a Truncated Species of Apolipoprotein B (B-31). A Unique Mutation That Helps to Define the Portion of the Apolipoprotein B Molecule Required for the Formation of Buoyant, Triglyceride-rich Lipoproteins. 1990.

Young, S G., et al. Familial Hypobetalipoproteinemia Caused By a Mutation in the Apolipoprotein B Gene That Results in a Truncated Species of Apolipoprotein B (B-31). A Unique Mutation That Helps to Define the Portion of the Apolipoprotein B Molecule Required for the Formation of Buoyant, Triglyceride-rich Lipoproteins. 1990.