Identification of the novel microdeletion Tyr163delAT and the first identified deletion/insertion mutant delGA; insTT in codon 329-330 of the factor X gene in homozygous patients with FX deficiency

Wulff, K. and Gnad, M. and Navarette, M. and Salazar-Sanchez, L. and Carillo, J. M. and Herrmann, F. H. (2003) Identification of the novel microdeletion Tyr163delAT and the first identified deletion/insertion mutant delGA; insTT in codon 329-330 of the factor X gene in homozygous patients with FX deficiency. In: 45th Annual Meeting of the American Society of Hematology, December 06-09, 2003, San Diego, California.

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Item Type: Conference or Workshop Item (UNSPECIFIED)
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Innere Medizin III (Hämatologie und Internistische Onkologie)
Depositing User: Petra Gürster
Date Deposited: 14 Jul 2021 09:53
Last Modified: 14 Jul 2021 09:53
URI: https://pred.uni-regensburg.de/id/eprint/38403

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