Associated Papers
Identification of recurrent variants implicated in disease in bicuspid aortic valve patients through whole-exome sequencing.
Chen S et al.
Human Genomics, 2022
RET c.1901G>A and Novel SLC12A3 Mutations in Familial Pheochromocytomas
Zhao L et al.
Genes, 2022
35627249 (PubMed )
Supplement: genes-13-00864-s001.zip › Supplementary_Material_S2.The_information_of_annotated_gene_mutations2.xlsx › ___
A Global Map of G Protein Signaling Regulation by RGS Proteins.
Masuho I et al.
Cell, 2020
33007266 (PubMed )
Supplement: mmc5.xlsx › RGS16
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