Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

X-linked agammaglobulinaemia. Mutation A1246G (R372G).

Allergologia et immunopathologia - 1 Jan 2000

Barón Ruiz I, Martín Mateos M A, Plaza Martín A M, Giner Muñoz M T, Piquer M, Domínguez O

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Agammaglobulinaemia Tyrosine Kinase
Share to Agammaglobulinemia
Share to Giardia
Share to Giardiasis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Growth and Development

Share to Immunoglobulins, Intravenous

Share to Lymphopenia

Share to Medical History Taking

Source

Identifiers

PMID: 20554104
DOI: 10.1016/j.aller.2010.02.007

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

X-linked agammaglobulinaemia. Mutation A1246G (R372G).PMID 20554104Read ↗

X-Linked AgammaglobulinemiaSemantic proximity Read ↗

[X-linked agammaglobulinemia].Semantic proximity Read ↗

[Widely divergent clinical phenotype of X-linked agammaglobulinemia in two cousins].Semantic proximity Read ↗

Genomics analysis of leukaemia predisposition in X-linked agammaglobulinaemia.Semantic proximity Read ↗

X-linked agammaglobulinemia and other immunoglobulin deficiencies.Semantic proximity Read ↗

Phenotypic variability: clinical presentation between the 6th year and the 60th year in a family with X-linked agammaglobulinemia.Semantic proximity Read ↗

The spectrum of mutations in Btk that cause X-linked agammaglobulinemia.Semantic proximity Read ↗

X-Linked Agammaglobulinemia Case with TH Domain Missense Mutation in Bruton Tyrosine Kinase.Semantic proximity Read ↗

[Genetic study of an X-linked agammaglobulinemia pedigree caused by an BTK mutation].Semantic proximity Read ↗

Extreme variation in X-linked agammaglobulinemia phenotype in a three-generation family.Semantic proximity Read ↗

A case of rare splice-site Bruton's tyrosine kinase mutation with atypical X-linked agammaglobulinemia.Semantic proximity Read ↗

A deep intronic BTK variant underlies X-linked agammaglobulinemia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.