DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency

Volk, T (author)

Pannicke, U (author)

Reisli, I (author)

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Bulashevska, A (author)

Ritter, J (author)

Bjorkman, A (author)

Karolinska Institutet

Schaffer, AA (author)

Fliegauf, M (author)

Sayar, EH (author)

Salzer, U (author)

Fisch, P (author)

Pfeifer, D (author)

Di Virgilio, M (author)

Cao, HZ (author)

Yang, F (author)

Zimmermann, K (author)

Keles, S (author)

Caliskaner, Z (author)

Guner, S (author)

Schindler, D (author)

Hammarstrom, L (author)

Karolinska Institutet

Rizzi, M (author)

Hummel, M (author)

Pan-Hammarstrom, Q (author)

Karolinska Institutet

Schwarz, K (author)

Grimbacher, B (author)

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 (creator_code:org_t)

2015-10-16

2015

English.

In: Human molecular genetics. - : Oxford University Press (OUP). - 1460-2083 .- 0964-6906. ; 24:25, s. 7361-7372

Related links:

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https://doi.org/10.1...

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• Journal article (peer-reviewed)