Associated Papers
Clinical and genetic diagnosis of a patient with focal segmental glomerulosclerosis due to a novel variant of the ANLN gene.
Zhang J et al.
Cen Case Reports, 2026
Effects of a novel ANLN E841K mutation associated with SRNS on podocytes and its mechanism.
Lin L et al.
Cell Communication and Signaling : Ccs, 2023
Sequencing of a Chinese tetralogy of Fallot cohort reveals clustering mutations in myogenic heart progenitors.
Tang CSM et al.
Jci Insight, 2022
34905512 (PubMed )
Supplement: jciinsight-7-152198-s012.xlsx › SupplTable8._Rec_PseudoCtCADD20
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