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

Aksu M. D., ÖZEN S., AKSU T., GÜREL A., ÇETİNKAYA A., Unal S.

TURKISH JOURNAL OF HEMATOLOGY, vol.42, no.1, pp.61-64, 2025 (SCI-Expanded)

• Publication Type: Article / Letter
• Volume: 42 Issue: 1
• Publication Date: 2025
• Doi Number: 10.4274/tjh.galenos.2025.2024.0373
• Journal Name: TURKISH JOURNAL OF HEMATOLOGY
• Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, CINAHL, MEDLINE, TR DİZİN (ULAKBİM)
• Page Numbers: pp.61-64
• Open Archive Collection: AVESIS Open Access Collection
• Hacettepe University Affiliated: Yes