Associated Papers
Predicting valuable missense variants with AlphaMissense in a multiple pulmonary infection patient.
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Clinical Case Reports, 2024
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Supplement: CCR3-12-e8453-s001.xlsx › SNP
RET c.1901G>A and Novel SLC12A3 Mutations in Familial Pheochromocytomas
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Genes, 2022
35627249 (PubMed )
Supplement: genes-13-00864-s001.zip › Supplementary_Material_S2.The_information_of_annotated_gene_mutations2.xlsx › ___
Sequencing of a Chinese tetralogy of Fallot cohort reveals clustering mutations in myogenic heart progenitors.
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Jci Insight, 2022
34905512 (PubMed )
Supplement: jciinsight-7-152198-s012.xlsx › SupplTable7._Rec_CADD20
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