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Extreme Phenotypic Variation in Siblings with Identical Homozygous Mutations Causing ADA2 Deficiency: A Case Series

Turkish Journal of Hematology
DOI: 10.4274/tjh.galenos.2025.2024.0373
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Aksu, M. D., Özen, S., Aksu, T., Gürel, A., Çetinkaya, A., & Ünal, Ş. (2025). Extreme Phenotypic Variation in Siblings with Identical Homozygous Mutations Causing ADA2 Deficiency: A Case Series. Turkish Journal of Hematology. Turkish Society of Hematology. https://doi.org/10.4274/tjh.galenos.2025.2024.0373

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