Proteomics Profiling to Distinguish DOCK8 Deficiency From Atopic Dermatitis
Dedicator of cytokinesis 8 deficiency is an autosomal recessive primary immune deficiency disease belonging to the group of hyperimmunoglobulinemia E syndrome (HIES). The clinical phenotype of dedicator of cytokinesis 8 (DOCK8) deficiency, characterized by allergic manifestations, increased infectio...
Enregistré dans:
Auteurs principaux: | Minnie Jacob, Afshan Masood, Zakiya Shinwari, Mai Abdel Jabbar, Hamoud Al-Mousa, Rand Arnaout, Bandar AlSaud, Majed Dasouki, Ayodele A. Alaiya, Anas M. Abdel Rahman |
---|---|
Format: | article |
Langue: | EN |
Publié: |
Frontiers Media S.A.
2021
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/d1f6d8850f3e45c4a80647f65242f9cb |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Defective Toll-Like Receptors Driven B Cell Response in Hyper IgE Syndrome Patients With STAT3 Mutations
par: Ruolan Gong, et autres
Publié: (2021) -
Hyper ige syndrome associated with novel dock8 heterozygous mutation: а case report
par: D. V. Osypchuk, et autres
Publié: (2020) -
Síndrome de hiper IgE, una enfermedad poco frecuente en edad adulta: Reporte de un caso
par: Aguilera S,Guillermo, et autres
Publié: (2015) -
A Novel Germline Heterozygous BCL11B Variant Causing Severe Atopic Disease and Immune Dysregulation
par: Henry Y. Lu, et autres
Publié: (2021) -
HYPER IMMUNOGLOBULIN E IGE SYNDROME (HIES) WITH PARTIAL T LYMPHOCYTES DEFICIENCY
par: Muhammad Hussain, et autres
Publié: (2019)