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Autor:
Belykh Natalia Anatolievna, Glotova Inna Aleksandrovna, Deeva Yuliya Vitalievna, Piznyur Inna Vladimirovna
Publikováno v:
Паёми Сино, Vol 26, Iss 4, Pp 700-709 (2024)
Wiskott-Aldrich syndrome (WAS) is a rare X-linked recessive disorder characterized by a triad of symptoms: immunodeficiency, thrombocytopenia, and eczema. It arises from a mutation in the gene encoding the WAS protein (WASp). The disease can present
Externí odkaz:
https://doaj.org/article/0f346c2d2fd040ac94f7acfa765451ce
