Associated Papers
Pharmaceuticals Promoting Premature Termination Codon Readthrough: Progress in Development.
Li S et al.
Biomolecules, 2023
37371567 (PubMed )
Supplement: biomolecules-13-00988-s001.zip › biomolecules-2391899-supplementary.xlsx › Sheet1
Variable readthrough responsiveness of nonsense mutations in hemophilia A.
Martorell L et al.
Haematologica, 2020
F8 gene mutation profile in Indian hemophilia A patients: Identification of 23 novel mutations and factor VIII inhibitor risk association.
Pinto P et al.
Mutation Research, 2016
Detection of factor VIII gene mutations by high-resolution melting analysis.
Laurie AD et al.
Clinical Chemistry, 2007
Effects of 7 hemoglobin variants on the measurement of glycohemoglobin by 14 analytical methods.
Lee ST et al.
Clinical Chemistry, 2007
The molecular aetiology of haemophilia A in a New Zealand patient group.
Laurie AD et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2007
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