Associated Papers
Rare loss-of-function variants in matrisome genes are enriched in Ebstein's anomaly.
Zhou Z et al.
Hgg Advances, 2024
38006208 (PubMed )
Supplement: mmc1.pdf
Whole genome sequencing identifies ANXA3 and MTHFR mutations in a large family with an unknown equinus deformity associated genetic disorder.
Zhang Z et al.
Molecular Biology Reports, 2016
Select a paper to view details