Literature DB >> 28087326

Autoimmune lymphoproliferative syndrome caused by homozygous FAS mutations with normal or residual protein expression.

Nourhen Agrebi1, Lamia Sfaihi Ben-Mansour2, Moez Medhaffar3, Sondes Hadiji3, Faten Fedhila4, Meriem Ben-Ali5, Najla Mekki6, Mongia Hachicha2, Sihem Barsaoui4, Mohamed-Ridha Barbouche7, Imen Ben-Mustapha6.   

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Year:  2017        PMID： 28087326     DOI： 10.1016/j.jaci.2016.11.033

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN： 0091-6749            Impact factor:   10.793


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  3 in total

Review 1.  Lessons from Genetic Studies of Primary Immunodeficiencies in a Highly Consanguineous Population.

Authors:  Mohamed-Ridha Barbouche; Najla Mekki; Meriem Ben-Ali; Imen Ben-Mustapha
Journal:  Front Immunol       Date:  2017-06-27       Impact factor: 7.561

2.  Stabilized β-Catenin Ameliorates ALPS-Like Symptoms of B6/lpr Mice.

Authors:  Xiaoxie Xu; Jun Huang; Mei Zhao; Huanpeng Chen; Jinhua Mo; Xiaoqing Zhou; Qiao Su; Bolan Yu; Zhaofeng Huang
Journal:  J Immunol Res       Date:  2017-11-09       Impact factor: 4.818

3.  Comprehensive Genetic Results for Primary Immunodeficiency Disorders in a Highly Consanguineous Population.

Authors:  Waleed Al-Herz; Janet Chou; Ottavia Maria Delmonte; Michel J Massaad; Wayne Bainter; Riccardo Castagnoli; Christoph Klein; Yenan T Bryceson; Raif S Geha; Luigi D Notarangelo
Journal:  Front Immunol       Date:  2019-01-15       Impact factor: 7.561
  3 in total

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