Associated Papers
GAPO syndrome: a comprehensive examination and review of 105 clinical cases.
Modafferi C et al.
Journal of Medical Genetics, 2025
Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies.
Bouzidi A et al.
Orphanet Journal of Rare Diseases, 2022
35551639 (PubMed )
Supplement: 13023_2022_2340_MOESM5_ESM.xlsx › Feuil1
GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletion.
Abdel-Hamid MS et al.
American Journal of Medical Genetics. Part A, 2019
Select a paper to view details