Work

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

Year: 2025

Type: article

Study design: Observational Study

Source: Journal of Pediatric Hematology/Oncology

DOI: 10.1097/mph.0000000000003008

Authors: Kökcü Karadag Sefika Ilknur, Karadağ Alpaslan Medine, Karadağ Hüseyin, Uğurtay Eda Turgut, Can Cansu, Yildiran Alisan

Institution: Ondokuz Mayıs University

Language: English

Topic: Complement system in diseases

Subfield: Immunology

Field: Immunology and Microbiology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W4408781875

FWCI: 0.884

Cites: 12

Cited by: 3

Related to: 10