Associated Papers
Genome-wide discovery of human splicing branchpoints.
Mercer TR et al.
Genome Research, 2015
25561518 (PubMed )
Supplement: supp_gr.182899.114_Supplemental_TableS3.xlsx › HGMD_predictedMotifs
Molecular Basis of KELnull Phenotype in Brazilians.
Boturão-Neto E et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2015
Genetic diversity of KELnull and KELel: a nationwide Austrian survey.
Körmöczi GF et al.
Transfusion, 2007
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