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Clinical Manifestations, Mutational Analysis, and Immunological Phenotype in Patients with RAG1/2 Mutations: First Cases Series from Mexico and Description of Two Novel Mutations

Journal of Clinical Immunology(2021)10.1007/s10875-021-01052-0Source: DataRank Database

Clinical Manifestations, Mutational Analysis, and Immunological Phenotype in Patients with RAG1/2 Mutations: First Cases Series from Mexico and Description of Two Novel Mutations is a research paper published in Journal of Clinical Immunology (2021). On theSindex it has a DataRank of 0. It has been cited 3 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access3 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (3 grants)Impact (FWCI 0.15)OA: greenTopics (52)IDs (PubMed, PMC, OpenAlex)Annotations (2)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (23)

Nina Pastor ORCID,Edith González‐Serrano,Marco Antonio Yamazaki‐Nakashimada ORCID,Selma Scheffler‐Mendoza ORCID,Laura Berrón‐Ruiz ORCID

Live enrichment

PubMed:33954879 PMC:PMC8319791 OpenAlex:https://openalex.org/W3131459613

Intramural NIH HHS

Grant: ZIA AI001222

Consejo Nacional de Ciencia y Tecnología

Division of Intramural Research, National Institute of Allergy and Infectious Diseases

FWCI

0.15

Citation Percentile

0.4%

Citation Trend

2023

2024

2026

greenLicense: https://www.springer.com/tdm

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/8319791

GREENhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319791

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/8319791

publisherhttps://link.springer.com/content/pdf/10.1007/s10875-021-01052-0.pdf

publisherhttps://link.springer.com/article/10.1007/s10875-021-01052-0/fulltext.html

Fields of Study

Immunodeficiency and Autoimmune DisordersImmune Cell Function and InteractionBlood disorders and treatmentsBiologyMedicineAdolescentChildDNA-Binding ProteinsFemaleHomeodomain ProteinsHumansImmunologic Deficiency SyndromesInfantLymphocytesMaleMexicoMutationNuclear ProteinsPhenotype

MeSH Terms

AdolescentChildDNA-Binding ProteinsFemaleHumansImmunologic Deficiency SyndromesInfantLymphocytesMaleMexicoMutationNuclear ProteinsPhenotypeHomeodomain Proteins

Keywords

Recombination-activating geneRAG2BiologyMissense mutationPhenotypeSevere combined immunodeficiencyPrimary immunodeficiencyMutationGeneticsImmunodeficiencyImmunologyGeneImmune systemRecombinationT lymphocytesSCIDPrimary ImmunodeficienciesOmenn SyndromeRag1/2

Sustainable Development Goals

SDG 0: Good health and well-being

Clinical Manifestations, Mutational Analysis, and Immunological Phenotype in Patients with RAG1/2 Mutations: First Cases Series from Mexico and Description of Two Novel Mutations

FAIR Checklist

Authors (23)

Funding (3 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)