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...

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מידע ביבליוגרפי

Principais autores:	Shahnaz Armin, Keyvan Ramezani, Bibi Shahin Shamsian, Zahra Chavoshzadeh, Maryam Eghbali, Alireza Zare Bidoki, Maryam Sadr, Mehrnaz Mesdaghi, Hooshang Gorjipour, Sepideh Razi, Nima Rezaei
פורמט:	Artigo
שפה:	Inglês
יצא לאור:	Tehran University of Medical Sciences 2020-05-01
סדרה:	Acta Medica Iranica
נושאים:	Hyper-IgM syndrome Class-switch recombination deficiency Mutation Immunodeficiency CD40 ligand gene (CD40LG) Hyper-immunoglobulin M (HIGM)
גישה מקוונת:	https://acta.tums.ac.ir/index.php/acta/article/view/7609
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