Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity

Lopez-Herrera, G (author)

Tampella, G (author)

Pan-Hammarstrom, Q (author)

Karolinska Institutet

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Herholz, P (author)

Trujillo-Vargas, CM (author)

Phadwal, K (author)

Simon, AK (author)

Moutschen, M (author)

Etzioni, A (author)

Mory, A (author)

Srugo, I (author)

Melamed, D (author)

Hultenby, K (author)

Karolinska Institutet

Liu, CH (author)

Karolinska Institutet

Baronio, M (author)

Vitali, M (author)

Philippet, P (author)

Dideberg, V (author)

Aghamohammadi, A (author)

Rezaei, N (author)

Enright, V (author)

Du, LK (author)

Karolinska Institutet

Salzer, U (author)

Eibel, H (author)

Pfeifer, D (author)

Veelken, H (author)

Stauss, H (author)

Lougaris, V (author)

Plebani, A (author)

Gertz, EM (author)

Schaffer, AA (author)

Hammarstrom, L (author)

Karolinska Institutet

Grimbacher, B (author)

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 (creator_code:org_t)

Elsevier BV, 2012

2012

English.

In: American journal of human genetics. - : Elsevier BV. - 1537-6605 .- 0002-9297. ; 32:2, s. 363-364

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• Journal article (peer-reviewed)