Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2, and HBB associated with haemoglobinopathies
Stella Tamana(Fundación Instituto Leloir), Petros Kountouris(Cyprus Institute of Neurology and Genetics), Faidatul Syazlin Abdul Hamid(Ministry of Health), Cornelis L. Harteveld(Leiden University Medical Center), Anna Minaidou(Cyprus Institute of Neurology and Genetics), Marina Kleanthous(Cyprus Institute of Neurology and Genetics), Norafiza Mohd Yasin(Institute for Medical Research), Andrea C. Kakouri(Cyprus Institute of Neurology and Genetics), Ezalia Esa(Institute for Medical Research), Joanne Traeger‐Synodinos(National and Kapodistrian University of Athens), Celeste Bento(Hospitais da Universidade de Coimbra), Bin Alwi Zilfalil(Hospital Universiti Sains Malaysia), Hashim Halim‐Fikri(Universiti Sains Malaysia), Coralea Stephanou(Agruicultural Research Institute), Irene Fylaktou(National and Kapodistrian University of Athens), Maria Xenophontos(Cyprus Institute of Neurology and Genetics)
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