Associated Papers
Comprehensive Screening of Genetic Variants in the Coding Region of F8 in Severe Hemophilia A Reveals a Relationship with Disease Severity in a Colombian Cohort.
Sarmiento Doncel S et al.
Life (basel, Switzerland), 2024
Variable readthrough responsiveness of nonsense mutations in hemophilia A.
Martorell L et al.
Haematologica, 2020
Genetic diagnosis in Hemophilia A from southern China: five novel mutations and one preimplantation genetic analysis.
Chen J et al.
International Journal of Laboratory Hematology, 2017
Identification of ten novel mutations in factor VIII gene: A study of a cohort of 52 haemophilia A patients.
Santacroce R et al.
Thrombosis Research, 2015
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