New mutant gene (transthyretin Arg 58) in cases with hereditary polyneuropathy detected by non-isotope method of single-strand conformation polymorphism analysis
- 15 October 1991
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 180 (1) , 380-385
- https://doi.org/10.1016/s0006-291x(05)81304-x
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Recent advances in the molecular pathology of familial amyloid polyneuropathyNeuromuscular Disorders, 1991
- DNA sequence polymorphisms in Alu repeatsGenomics, 1990
- Two novel variants of transthyretin identified in Japanese cases with familial amyloidotic polyneuropathy: Transthyretin (Glu42 to Gly) and transthyretin (Ser50 to Arg)Biochemical and Biophysical Research Communications, 1990
- A novel variant of transthyretin (Tyr114 to Cys) deduced from the nucleotide sequences of gene fragments from familial amyloidotic polyneuropathy in Japanese sibling casesBiochemical and Biophysical Research Communications, 1990
- Nonradioactive DNA detection on Southern blots by enzymatically triggered chemiluminescenceAnalytical Biochemistry, 1990
- Direct sequencing of the gene for Maryland/German familial amyloidotic polyneuropathy type II and genotyping by allele-specific enzymatic amplificationGenomics, 1989
- Chemiluminescent detection of DNA: application for DNA sequencing and hybridizationNucleic Acids Research, 1989
- Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis.Journal of Clinical Investigation, 1986
- THE GENETIC AMYLOIDOSESMedicine, 1969