(Q55670920)

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Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B-severe combined immune deficiency or Omenn syndrome

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title

Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B-severe combined immune deficiency or Omenn syndrome (English)

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1 reference

4

N Wulffraat

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author name string

B Corneo

series ordinal

1

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D Moshous

series ordinal

2

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T Güngör

series ordinal

3

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P Philippet

series ordinal

5

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F L Le Deist

series ordinal

6

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A Fischer

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7

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J P de Villartay

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8

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language of work or name

English

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publication date

1 May 2001

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published in

Blood

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volume

97

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page(s)

2772-6

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issue

9

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Identifiers

DOI

10.1182/BLOOD.V97.9.2772

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PubMed ID

11313270

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(Q55670920)

Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B-severe combined immune deficiency or Omenn syndrome

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