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Genomics|October 1, 1989
Direct sequencing of the gene for Maryland/German familial amyloidotic polyneuropathy type II and genotyping by allele-specific enzymatic amplificationW C Nichols, J J Liepnieks, V A McKusick, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 10, 2004
A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathyLawreen Heller Connors, Taro Yamashita, Masahide Yazaki, et al.
Cardiology in Review|March 24, 2021
Genetic Risk Assessment for Atherosclerotic Cardiovascular Disease: A Guide for the General CardiologistMatthew J Belanger, Erik M Kelly, Usman A Tahir, et al.
The Journal of Laboratory and Clinical Medicine|March 1, 1991
Senile cardiac amyloidosis associated with homozygosity for a transthyretin variant (ILE-122)W C Nichols, J J Liepnieks, E L Snyder, et al.
Biorxiv : the Preprint Server for Biology|July 14, 2025
High-Throughput Evaluation of Cryoprotective Agents for Mixture Effects That Reduce ToxicityNima Ahmadkhani, Cameron Sugden, James D Benson, et al.
Cryobiology|September 17, 2025
High-throughput evaluation of cryoprotective agents for mixture effects that reduce toxicityNima Ahmadkhani, Cameron Sugden, James D Benson, et al.
American Journal of Medical Genetics|October 1, 1986
Molecular detection of carriers of hereditary amyloidosis in a Swedish-American familyM R Wallace, P M Conneally, G L Long, et al.
Molecular Vision|January 4, 2018
A targeted approach to genome-wide studies reveals new genetic associations with central corneal thicknessMatthew D Benson, Chiea C Khor, Philip J Gage, et al.
Lancet (London, England)|January 4, 1975
Neuropathy, M components, and amyloidM D Benson, A S Cohen, K D Brandt, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|May 1, 1985
Isolation and characterization of amyloid protein AA in the Abyssinian catS P DiBartola, M D Benson, F E Dwulet, et al.
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