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. |
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Zdroj: | In Clinical Immunology October 2017 183:17-23 |
Databáze: | ScienceDirect |
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