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Severe XLP phenotype caused by a novel intronic mutation in the SH2D1A gene.

Tóth, 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

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Item Type: Article
Subjects: R Medicine / orvostudomány > RZ Other systems of medicine / orvostudomány egyéb területei
Depositing User: Dr Beáta Lajszné Tóth
Date Deposited: 10 Sep 2015 12:31
Last Modified: 03 Apr 2023 08:30
URI: http://real.mtak.hu/id/eprint/26283

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