Paediatrics

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

January 7, 2025 January 7, 2025

Turk J Haematol. 2025 Jan 7. doi: 10.4274/tjh.galenos.2025.2024.0373. Online ahead of print.

NO ABSTRACT

PMID:39764790 | DOI:10.4274/tjh.galenos.2025.2024.0373

John Joseph

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