• A biallelic ANTXR1 variant expands the anthrax toxin receptor associated phenotype to tooth agenesis
• ANTXR1 deficiency promotes fibroblast senescence: implications for GAPO syndrome as a progeroid disorder
• Antxr1, Which is a Target of Runx2, Regulates Chondrocyte Proliferation and Apoptosis
• Changing facial features in a child with GAPO syndrome caused by novel mutation in the ANTXR1 gene and uniparental disomy of chromosome 2
• Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
• Converging physiological roles of the anthrax toxin receptors
• Dental Management of Siblings with GAPO Syndrome
• Disruption of anthrax toxin receptor 1 in pigs leads to a rare disease phenotype and protection from senecavirus A infection
• Distribution of <em>TGFBI</em> variants in patients with early onset glaucoma
• Endoscopic Optic Nerve Decompression in a Hamamy Syndrome Patient With Bilateral Optic Canal Stenosis
• GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletion
• GAPO syndrome with craniosynostosis and intracranial hypertension
• GAPO syndrome: a novel variant in ANTXR1 gene
• GAPO syndrome: a rare genodermatosis presenting with unique features
• Hypotony Maculopathy After Trabeculectomy in a Patient With GAPO Syndrome
• Ligand Binding to the Collagen VI Receptor Triggers a Talin-to-RhoA Switch that Regulates Receptor Endocytosis
• Prenatal onset GAPO syndrome with a novel ANTXR1 variant in an Indian child: Expansion of the phenotype & literature review
• Telogen hair loss and androgenetic-like alopecia in GAPO syndrome
• Two siblings with GAPO syndrome: a novel missense variant in ANTXR1
• Two siblings with GAPO syndrome: Ophthalmic presentation and histopathologic findings