Associated Papers
Expanding the Molecular Spectrum of MMP21 Missense Variants: Clinical Insights and Literature Review.
Pasquetti D et al.
Genes, 2025
De novo disruptive heterozygous MMP21 variants are potential predisposing genetic risk factors in Chinese Han heterotaxy children.
Qin XJ et al.
Human Genomics, 2022
36123719 (PubMed )
Supplement: 40246_2022_409_MOESM4_ESM.xlsx › MMP21_variants
A Novel Nonsense MMP21 Variant Causes Dextrocardia and Congenital Heart Disease in a Han Chinese Patient.
Yuan ZZ et al.
Frontiers in Cardiovascular Medicine, 2020
Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families.
Akawi N et al.
Nature Genetics, 2015
Select a paper to view details