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Abbravation: Journal of Human Genetics

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Nature Publishing Group

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1435-232X

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Genetic polymorphism of the a subunit of human coa

Authors: Toshinori Nishigaki Keiichi Omoto Takeo Juji
Publish Date: 1981/09
Volume: 26, Issue: 3, Pages: 237-
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Abstract

Thank you for visiting naturecom You are using a browser version with limited support for CSS To obtain the best experience we recommend you use a more up to date browser or turn off compatibility mode in Internet Explorer In the meantime to ensure continued support we are displaying the site without styles and JavaScriptPolymorphism of the A subunit of human coagulation factor XIII was investigated in a total of 561 plasma samples from unrelated adult Japanese using an agarose gel electrophoresis followed by a fluorescent technique for the localization of transglutaminase activity Three common phenotypes were observed which corresponded to the types 1 21 and 2 reported by Board 1979 in Australians The family material from 23 matings with 60 children indicated that these phenotypes are controlled by a pair of autosomal codominant alleles The estimated allele frequencies of F13A1 and F13A2 were 0887 and 0113 respectively


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  8. Isolation of human chromosome 21-specific cosmids and their uses in mapping of cosmid contigs on chromosomal subregions
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  11. Dynamin 2 gene is a novel susceptibility gene for late-onset Alzheimer disease in non- APOE -ε4 carriers
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  15. Molecular cloning of a novel human gene ( SIRP-B2 ) which encodes a new member of the SIRP/SHPS-1 protein family
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