APA (7th ed.) Citation

Bakır, D. B., Atay, Ö., Yağmur, H., Kabadayı, G., Kocabey, M., Asilsoy, S., & Uzuner, N. (2025). Expanding the clinical spectrum of pediatric ataxia-telangiectasia: A case series of novel genetic variants, lupus vulgaris, and hyper-IgM phenotypes. Orphanet Journal of Rare Diseases, 20(1), 1. https://doi.org/10.1186/s13023-025-03942-7

Chicago Style (17th ed.) Citation

Bakır, Damla Baysal, Özge Atay, Halime Yağmur, Gizem Kabadayı, Mehmet Kocabey, Suna Asilsoy, and Nevin Uzuner. "Expanding the Clinical Spectrum of Pediatric Ataxia-telangiectasia: A Case Series of Novel Genetic Variants, Lupus Vulgaris, and Hyper-IgM Phenotypes." Orphanet Journal of Rare Diseases 20, no. 1 (2025): 1. https://doi.org/10.1186/s13023-025-03942-7.

MLA (9th ed.) Citation

Bakır, Damla Baysal, et al. "Expanding the Clinical Spectrum of Pediatric Ataxia-telangiectasia: A Case Series of Novel Genetic Variants, Lupus Vulgaris, and Hyper-IgM Phenotypes." Orphanet Journal of Rare Diseases, vol. 20, no. 1, 2025, p. 1, https://doi.org/10.1186/s13023-025-03942-7.