Tracing a Rare Genetic Disease: Familial Congenital CD59 Deficiency and Carrier Cases Identified through Village Screening: Erratum.

IF 0.9 4区医学 Q4 HEMATOLOGY

Journal of Pediatric Hematology/Oncology Pub Date : 2025-07-01 Epub Date: 2025-06-23 DOI:10.1097/MPH.0000000000003054

Şefika Lknur Kökcü Karadağ, Medine Karadağ Alparslan, Hüseyin Karadağ, Eda Turgut Uğurtay, Cansu Can, Alisan Yildiran

引用次数: 0

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追踪一种罕见的遗传性疾病：家族性先天性CD59缺乏和通过村筛查确定的携带者病例：勘误。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Journal of Pediatric Hematology/Oncology 医学-小儿科

CiteScore

1.90

自引率

8.30%

发文量

415

审稿时长

2.5 months

期刊介绍： Journal of Pediatric Hematology/Oncology (JPHO) reports on major advances in the diagnosis and treatment of cancer and blood diseases in children. The journal publishes original research, commentaries, historical insights, and clinical and laboratory observations.