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Jump to: Article Number of items: 1. ArticleTóth, Beáta and Soltész, Beáta and Gyimesi, Edit and Csorba, Gabriella and Veres, Ágota and Lányi, Árpád and Kovács, Gábor and Maródi, László and Erdős, Melinda (2015) Severe XLP phenotype caused by a novel intronic mutation in the SH2D1A gene. Journal of clinical immunology (35). pp. 26-31. ISSN 1573-2592 |