Relevance of biallelic vs monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

Salzer, US (author)

Bacchelli, C (author)

Buckridge, S (author)

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Pan-Hammar-Strom, Q (author)

Jennings, S (author)

Lougaris, V (author)

Bergbreiter, A (author)

Hagena, T (author)

Birmelin, J (author)

Plebani, A (author)

Webster, ADB (author)

Peter, HH (author)

Suez, D (author)

Chapel, H (author)

Maclean-Tooke, A (author)

Spickett, GP (author)

Anover-Sombke, S (author)

Ochs, HD (author)

Urschel, S (author)

Belohradsky, BH (author)

Ugrinovic, S (author)

Kumararatne, DS (author)

Lawrence, TC (author)

Holm, AM (author)

Franco, JL (author)

Schulze, I (author)

Schneider, P (author)

Gertz, ME (author)

Schaffer, AA (author)

Hammarstrom, L (author)

Karolinska Institutet

Thrasher, AJ (author)

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 (creator_code:org_t)

2008

2008

English.

In: CLINICAL AND EXPERIMENTAL IMMUNOLOGY. - 0009-9104. ; 154, s. 207-208

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