Evidence map›Paper›PMID 33733381›Full record

ArticleJournal of clinical immunology2021

A New Missense Mutation in CD79B Leads to Autosomal Recessive Agammaglobulinemia in Two Siblings.

Steve Genebrier, Mathieu Fusaro, Nathalie Lambert, Sylvie Roullaud, Frédéric Millot, Capucine Picard

Abstract readCase ReportsLetter
PubMed Publisher
In one paragraph

Article in Journal of clinical immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 62% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 3 countries.

Steve GenebrierStudy Center for Primary Immunodeficiencies, Necker Hospital for Sick Children - Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Mathieu FusaroStudy Center for Primary Immunodeficiencies, Necker Hospital for Sick Children - Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Nathalie LambertStudy Center for Primary Immunodeficiencies, Necker Hospital for Sick Children - Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Sylvie RoullaudPediatric Department, CH Angouleme, Angouleme, France.
Frédéric MillotPediatric Department, University Hospital, Poitiers, France.
Capucine PicardStudy Center for Primary Immunodeficiencies, Necker Hospital for Sick Children - Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France. capucine.picard@inserm.fr.ORCID 0000-0001-8788-5056
Assistance Publique – Hôpitaux de Paris · FRHôpital Necker-Enfants Malades · FRInserm · FRUniversité de Poitiers · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AgammaglobulinemiaCD79 AntigensGenes, RecessiveHumansInfantInfant, NewbornMaleMutation, MissensePedigreeSiblingsCD79 AntigensCD79B protein, human

Identifiers

PMID33733381
OpenAlexW3138697693

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.