Novel CD40LG Mutation in Two Cousins With Immunoglobulin Class Switch Recombinant Deficiency

The hyper-immunoglobulin M (HIGM) syndrome comprises a group of rare inherited immunodeficiency disorders characterized by normal or elevated levels of serum IgM with low or absent levels of serum IgG, IgA, and IgE. Patients with this syndrome usually present with a history of recurrent infections o...

Celý popis

Podrobná bibliografie

Hlavní autoři:	Shahnaz Armin, Keyvan Ramezani, Bibi Shahin Shamsian, Zahra Chavoshzadeh, Maryam Eghbali, Alireza Zare Bidoki, Maryam Sadr, Mehrnaz Mesdaghi, Hooshang Gorjipour, Sepideh Razi, Nima Rezaei
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Tehran University of Medical Sciences 2020-05-01
Edice:	Acta Medica Iranica
Témata:	Hyper-IgM syndrome Class-switch recombination deficiency Mutation Immunodeficiency CD40 ligand gene (CD40LG) Hyper-immunoglobulin M (HIGM)
On-line přístup:	https://acta.tums.ac.ir/index.php/acta/article/view/7609
Tagy:	Přidat tag Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!