Clinical, immunological and genetic findings of a large tunisian series of major histocompatibility complex class II deficiency patients.
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Lessons from Genetic Studies of Primary Immunodeficiencies in a Highly Consanguineous Population.Sequential asymptomatic enterovirus infections in a patient with major histocompatibility complex class II primary immunodeficiencyDisseminated Bacillus Calmette-Guérin (BCG) infection following allogeneic hematopoietic stem cell transplant in a patient with Bare Lymphocyte Syndrome type II.Modern management of primary T-cell immunodeficiencies.A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients.Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients.A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients.Hypoxemic Bronchiolitis Related to Major Histocompatibility Class II Deficiency.
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P2860
Clinical, immunological and genetic findings of a large tunisian series of major histocompatibility complex class II deficiency patients.
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2013 nî lūn-bûn
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Clinical, immunological and ge ...... class II deficiency patients.
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type
label
Clinical, immunological and ge ...... class II deficiency patients.
@en
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Clinical, immunological and ge ...... class II deficiency patients.
@en
P2093
P2860
P1476
Clinical, immunological and ge ...... class II deficiency patients.
@en
P2093
Beya Larguèche
Emna Dhemaied
Fethi Mellouli
Imen Ben-Mustapha
Jalel Chemli
Jihène Bouguila
Khaoula Ben-Farhat
Lamia Ben-Mansour
Meriem Ben-Ali
Mohamed Béjaoui
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P2888
P304
P356
10.1007/S10875-013-9863-8
P577
2013-01-13T00:00:00Z
P6179
1008689646