(Q33937028)

30 July 2017

title

Autoimmunity due to RAG deficiency and estimated disease incidence in RAG1/2 mutations (English)

1 reference

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11

Lynn B Jorde

1 reference

30 July 2017

12

Luigi D Notarangelo

1 reference

30 July 2017

10

John F Bohnsack

1 reference

30 July 2017

Karin Chen

1

1 reference

30 July 2017

Wilfred Wu

2

1 reference

30 July 2017

Divij Mathew

3

1 reference

30 July 2017

Yuhua Zhang

4

1 reference

30 July 2017

Sarah K Browne

5

1 reference

30 July 2017

Lindsey B Rosen

6

1 reference

30 July 2017

Meghann P McManus

7

1 reference

30 July 2017

Michael A Pulsipher

8

1 reference

30 July 2017

Mark Yandell

9

1 reference

30 July 2017

Jolan E Walter

13

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30 July 2017

language of work or name

English

0 references

publication date

25 January 2014

1 reference

The Journal of Allergy and Clinical Immunology

30 July 2017

published in

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30 July 2017

volume

133

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30 July 2017

issue

3

1 reference

30 July 2017

page(s)

880-2.e10

1 reference

Newborn screening for severe combined immunodeficiency and T-cell lymphopenia in California: results of the first 2 years

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107635

The long quest for neonatal screening for severe combined immunodeficiency

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107635

Recombination centres and the orchestration of V(D)J recombination

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107635

Anti-cytokine autoantibodies are associated with opportunistic infection in patients with thymic neoplasia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107635

More than just SCID--the phenotypic range of combined immunodeficiencies associated with mutations in the recombinase activating genes (RAG) 1 and 2.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107635

RAG-dependent primary immunodeficiencies.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107635

Anti-interferon autoantibodies in autoimmune polyendocrinopathy syndrome type 1

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107635

A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107635

Highly variable clinical phenotypes of hypomorphic RAG1 mutations

5 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24472623

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

An integrated map of genetic variation from 1,092 human genomes

1 reference

4 November 2023

https://opencitations.net/index/coci/api/v1/citations/10.1038/NATURE11632

Identifiers

DOI

10.1016/J.JACI.2013.11.038

1 reference

30 July 2017

1 reference

30 July 2017

1 reference