Merrill D. Benson

Hereditary renal amyloidosis with a novel variant fibrinogen.

J. Liepnieks, M. Benson, T. Uemichi, 1994, The Journal of clinical investigation.

Identification of a novel substitution in the constant region of a gene coding for an amyloidogenic kappa1 light chain.

M. Skinner, J. Liepnieks, M. Benson, 1999, Biochimica et biophysica acta.

A novel apolipoprotein A-1 variant, Arg173Pro, associated with cardiac and cutaneous amyloidosis.

J. Liepnieks, M. Benson, M D Benson, 1999, Biochemical and biophysical research communications.

Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1.

J. Liepnieks, M. Benson, M. Delpech, 1999, The American journal of pathology.

The x-ray crystal structure refinements of normal human transthyretin and the amyloidogenic Val-30-->Met variant to 1.7-A resolution.

J. Hamilton, L. Steinrauf, B. Braden, 1993, The Journal of biological chemistry.