Associated Papers
A rare case of coronin-1A deficiency with IgM dominant membranoproliferative glomerulonephritis.
Ural Z et al.
Cen Case Reports, 2025
Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits.
Yuan B et al.
Genome Medicine, 2022
36180924 (PubMed )
Supplement: 13073_2022_1113_MOESM1_ESM.xlsx › Table_S6
Recurrent viral infections associated with a homozygous CORO1A mutation that disrupts oligomerization and cytoskeletal association.
Yee CS et al.
The Journal of Allergy and Clinical Immunology, 2016
Select a paper to view details