F8 c.671-5_724del

Variant ID: X-154213025-GCAGCATCCCTATCCTGCATCAAGGAGTTCTTTGTTTCTGAGTGCCAACTTTTCCCTGAT-G

NM_000132.3(F8):c.671-5_724del

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Assessment of the F9 genotype-specific FIX inhibitor risks and characterisation of 10 novel severe F9 defects in the first molecular series of Argentinian patients with haemophilia B.

Thrombosis And Haemostasis
Radic, Claudia Pamela CP; Rossetti, Liliana Carmen LC; Abelleyro, Miguel Martín MM; Candela, Miguel M; Pérez Bianco, Raúl R; de Tezanos Pinto, Miguel M; Larripa, Irene Beatriz IB; Goodeve, Anne A; De Brasi, Carlos Daniel C
Publication Date: 2013-01

Variant appearance in text: FVIII: 520_724del
PubMed Link: 23093250
Variant Present in the following documents:
  • Main text
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