The amplification of Factor VIII gene-specific sequences, obtained by polymerase chain reaction, was used for hemophilia A carrier detection. Exon 24 sequences were employed in the carrier status determination of a missense mutation causing severe hemophilia A in two unrelated patients. After agarose gel electrophoresis, the digested DNA was subjected to quantitative determination of fluorescence. This technique significantly improves the digest analysis.

Direct detection of a missense mutation causing severe hemophilia A by PCR amplification and fluorescence scanning.

MARCHETTI, Giovanna;GEMMATI, Donato;VOLINIA, Stefano;BERNARDI, Francesco
1990

Abstract

The amplification of Factor VIII gene-specific sequences, obtained by polymerase chain reaction, was used for hemophilia A carrier detection. Exon 24 sequences were employed in the carrier status determination of a missense mutation causing severe hemophilia A in two unrelated patients. After agarose gel electrophoresis, the digested DNA was subjected to quantitative determination of fluorescence. This technique significantly improves the digest analysis.
1990
Marchetti, Giovanna; Gemmati, Donato; Patracchini, P; Volinia, Stefano; Castagnoli, A; Tosi, B; Capelli, M; Bernardi, Francesco
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/1682703
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