Associated Papers
A novel splice-altering frameshift variant in the COL1A1 gene underlies osteogenesis imperfecta type I: molecular characterization of a four-generation Chinese pedigree and literature review.
He D et al.
Human Genomics, 2025
40887625 (PubMed )
Supplement: 40246_2025_816_MOESM2_ESM.xlsx › Sheet1
Association of osteogenesis imperfecta and glaucoma: case report.
Alpogan O
Ophthalmic Genetics, 2023
COL1A1 novel splice variant in osteogenesis imperfecta and splicing variants review: A case report.
Dirani M et al.
Frontiers in Surgery, 2022
36338653 (PubMed )
Supplement: Table1.xlsx › Sup_tab1
Molecular Outcome, Prediction, and Clinical Consequences of Splice Variants in COL1A1, Which Encodes the proα1(I) Chains of Type I Procollagen.
Schleit J et al.
Human Mutation, 2015
Osteogenesis imperfecta and primary open angle glaucoma: genotypic analysis of a new phenotypic association.
Wallace DJ et al.
Molecular Vision, 2014
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