(Q43524710)

24 November 2017

title

Autosomal recessive agammaglobulinemia: the third case of Igβ deficiency due to a novel non-sense mutation (English)

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24 November 2017

Vassilios Lougaris

1

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24 November 2017

Massimiliano Vitali

2

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24 November 2017

Manuela Baronio

3

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24 November 2017

Daniele Moratto

4

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24 November 2017

Giacomo Tampella

5

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24 November 2017

Augusto Biasini

6

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24 November 2017

Raffaele Badolato

7

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24 November 2017

Alessandro Plebani

8

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24 November 2017

publication date

11 April 2014

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Journal of Clinical Immunology

24 November 2017

published in

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24 November 2017

volume

34

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24 November 2017

issue

4

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24 November 2017

page(s)

425-427

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https://scigraph.springernature.com/pub.10.1007/s10875-014-0033-4

24 November 2017

exact match

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cites work

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Genetic analysis of patients with defects in early B-cell development

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Primary B cell immunodeficiencies: comparisons and contrasts

21 January 2018

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Mutations in the mu heavy-chain gene in patients with agammaglobulinemia

21 January 2018

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Clinical and molecular analysis of patients with defects in micro heavy chain gene.

21 January 2018

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Mutations in the human lambda5/14.1 gene result in B cell deficiency and agammaglobulinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0033-4

Mutations in Igalpha (CD79a) result in a complete block in B-cell development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0033-4

Novel Igalpha (CD79a) gene mutation in a Turkish patient with B cell-deficient agammaglobulinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0033-4

Mutations of the Igbeta gene cause agammaglobulinemia in man.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0033-4

Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0033-4

An essential role for BLNK in human B cell development

21 January 2018

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Agammaglobulinemia and absent B lineage cells in a patient lacking the p85α subunit of PI3K.

21 January 2018

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Neutropenia associated with primary immunodeficiency syndromes

21 January 2018

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Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0033-4

Cutting edge: a hypomorphic mutation in Igbeta (CD79b) in a patient with immunodeficiency and a leaky defect in B cell development

21 January 2018

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12 December 2020

Repertoire selection by pre-B-cell receptors and B-cell receptors, and genetic control of B-cell development from immature to mature B cells

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12 December 2020

The roles of preB cell receptor in early B cell development and its signal transduction

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12 December 2020

X-linked agammaglobulinemia: report on a United States registry of 201 patients

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12 December 2020

Neutropenia in patients with primary antibody deficiency disorders.

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12 December 2020

10.1007/S10875-014-0033-4

Identifiers

DOI

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Dimensions Publication ID

24 November 2017

1047747121

0 references

1 reference