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ASCIA‐P69: A NOVEL AICDA MUTATION IN A CASE OF AUTOSOMAL RECESSIVE HYPER‐IGM SYNDROME, GROWTH HORMONE DEFICIENCY AND AUTOIMMUNITY
Author(s) -
Kashef Sara,
Fazel Ali,
Aleyasin Soheila,
Harsini Sara,
Karamizadeh Zohreh,
Zoghi Samaneh,
Flores Stefanie Klaver,
Boztug Kaan,
Rezaei Nima
Publication year - 2016
Publication title -
internal medicine journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.596
H-Index - 70
eISSN - 1445-5994
pISSN - 1444-0903
DOI - 10.1111/imj.69_13197
Subject(s) - medicine , activation induced (cytidine) deaminase , primary immunodeficiency , immunology , gene mutation , common variable immunodeficiency , endocrinology , mutation , antibody , genetics , immunoglobulin class switching , biology , gene , b cell , immune system