Rare splicing defects of FAS underly severe recessive autoimmune lymphoproliferative syndrome

Autor: Agrebi, N., Ben-Mustapha, I., Matoussi, N., Dhouib, N., Ben-Ali, M., Mekki, N., Ben-Ahmed, M., Larguèche, B., Ben Becher, S., Béjaoui, M., Barbouche, M.R.
Zdroj: In Clinical Immunology October 2017 183:17-23
Databáze: ScienceDirect