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
Identification of a novel WNK4 mutation in Chinese patients with pseudohypoaldosteronism type II.
Zhang C et al.
Nephron. Physiology, 2011
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