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- W2078136449 abstract "We have performed genetic analysis on seven Japanese families with type I antithrombin (AT) deficiency by the polymerase chain reaction (PCR)/direct DNA sequencing method. Five distinct mutations including two novel ones were identified in six of seven families. All subjects investigated were heterozygous for the mutations. In one family, however, no genetic abnormality was found within the analyzed DNA sequences." @default.
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- W2078136449 date "1998-06-01" @default.
- W2078136449 modified "2023-09-27" @default.
- W2078136449 title "Genetic Analysis of Mutations in Seven Japanese Families with Type I Antithrombin Deficiency" @default.
- W2078136449 doi "https://doi.org/10.1055/s-2007-995847" @default.
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