@misc{indiciae04fe04dc8d5c,
  title = {Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy.},
  author = {Miriam Ehrenberg and Maayan Avraham and Sandeep Sarma Asodu and Abigail R Moye and Riccardo Sangermano and Leah Rizel and Tahleel Ali-Nasser and Ifat Sher and David Gurwitz and Katherine R Chao and Antonio Rivera and Andrew R Webster and Carlo Rivolta and Hadas Newman and Eran Pras and Ygal Rotenstreich and Eyal Banin and Eric A Pierce and Dinah Zur and Gavin Arno and Kinga M Bujakowska and Siying Lin and Dror Sharon and Tamar Ben-Yosef},
  year = {2025},
  doi = {10.1016/j.gim.2025.101401},
  url = {https://pubmed.ncbi.nlm.nih.gov/40079362/},
  note = {Source identifier: 40079362}
}