Is microsomal triglyceride transfer protein the missing link in abetalipoproteinemia?
Robert L. Hamilton, Richard J. Havel – 1 August 1993 – In the study reported by Wetterau et al., a recently characterized heterodimeric protein called microsomal triglyceride transfer protein was undetectable on immunoblotting of samples from intestinal biopsies of human subjects with the genetic disorder abetalipoproteinemia. With only one fourth to one fifth the soluble proteins of homogenized intestinal biopsy specimens of normal human subjects and patients with different fat‐absorption defects, the 88‐kD subunit of microsomal triglyceride transfer protein was clearly detectable.