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PMID: 3003621 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Familial amyloidotic polyneuropathy diagnosed by cloned human prealbumin cDNA.

Neurology ·Vol. 36 ·No. 2 ·1986-02-00 ·Pages 298-301

Mita S, Maeda S, Ide M, Tsuzuki T, Shimada K, Araki S

Abstract

A diagnosis of familial amyloidotic polyneuropathy (FAP) can be made by use of restriction endonuclease NsiI, a cloned human prealbumin cDNA and Southern blot procedures. Digests of DNAs from 10 disease-free individuals showed two bands (6.6 kb and 3.2 kb) complementary to a human prealbumin cDNA, whereas digests from 11 individuals with FAP exhibited two additional bands (5.1 kb and 1.5 kb). We interpret these changes in pattern to be the result of a restriction site for NsiI located in the altered codon and associated with the mutant prealbumin gene. All these individuals with FAP were heterozygous for the prealbumin gene, carrying one normal and one mutant gene.

MeSH Terms
Adult Amyloidosis/diagnosis,genetics Base Sequence DNA Restriction Enzymes DNA, Recombinant Female Genetic Linkage Humans Male Pedigree Peripheral Nervous System Diseases/diagnosis,genetics Prealbumin/genetics
Chemicals
DNA, Recombinant Prealbumin DNA Restriction Enzymes
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Mita S
Maeda S
Ide M
Tsuzuki T
Shimada K
Araki S
Article Info
Journal
Neurology
Abbr.
Neurology
ISSN
0028-3878
Published
1986-02-00
Pages
298-301
Language
English
Region
United States
NLM ID
0401060
Subset
IM
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