Associated Papers
Molecular analysis of human solute carrier SLC26 anion transporter disease-causing mutations using 3-dimensional homology modeling.
Rapp C et al.
Biochimica Et Biophysica Acta. Biomembranes, 2017
Functional analysis of nonsynonymous single nucleotide polymorphisms in human SLC26A9.
Chen AP et al.
Human Mutation, 2012
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