Purine nucleoside phosphorylase (PNP) deficiency: across-the-board severe combined immunodeficiency

Abstract Background Purine nucleoside phosphorylase (PNP) deficiency is a rare, autosomal recessive, inborn error of immunity. It is characterized by progressive immune abnormalities ranging from severe combined immunodeficiency (SCID) to combined immunodeficiency less profound than SCID, neurologic...

Täydet tiedot

Tallennettuna:

Bibliografiset tiedot
Päätekijät:	Engy A. Chohayeb, Sohilla Lotfy, Rabab E. El Hawary, Safa S. Meshaal, Iman A. Mansour, Nermeen M. Galal, Aisha M. Elmarsafy
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	SpringerOpen 2024-09-01
Sarja:	Egyptian Journal of Medical Human Genetics
Aiheet:	Hematopoietic stem cell transplantation (HSCT) Inborn errors of immunity (IEI) Purine nucleoside phosphorylase deficiency (PNP) Severe combined immunodeficiency (SCID)
Linkit:	https://doi.org/10.1186/s43042-024-00581-8
Tagit:	Lisää tagi Ei tageja, Lisää ensimmäinen tagi!

Purine nucleoside phosphorylase (PNP) deficiency: across-the-board severe combined immunodeficiency

Samankaltaisia teoksia