Revised analysis of amino acid replacement in a prealbumin variant (SKO-III) associated with familial amyloidotic polyneuropathy of jewish origin
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference5 articles.
1. The Metabolic Basis of Inherited Disease;Glenner,1978
2. Identification of amyloid prealbumin variant in familial amyloidotic polyneuropathy (Japanese type)
3. The Amino Acid Sequence of Human Plasma Prealbumin
4. Structure of prealbumin: Secondary, tertiary and quaternary interactions determined by Fourier refinement at 1.8 Å
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