Associated Papers
A novel variant in the COL4A3 gene: etiology of Alport syndrome type 2 in a 38-year-old male with suspected hereditary kidney disease.
Sienes Bailo P et al.
Advances in Laboratory Medicine, 2021
Structural and functional roles of small group-conserved amino acids present on helix-H7 in the β(2)-adrenergic receptor.
Arakawa M et al.
Biochimica Et Biophysica Acta, 2011
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