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A De Novo Mutation in ACTC1 and a TTN Variant Linked to a Severe Sporadic Infant Dilated Cardiomyopathy Case

Case Reports in Genetics(2024)10.1155/crig/9517735Source: DataRank Database

A De Novo Mutation in ACTC1 and a TTN Variant Linked to a Severe Sporadic Infant Dilated Cardiomyopathy Case is a research paper published in Case Reports in Genetics (2024). On theSindex it has a DataRank of 0. It has been cited 1 time.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access1 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (2 grants)Impact (FWCI 0.30)OA: goldTopics (14)IDs (PubMed, OpenAlex)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 (10)

Norma Balderrábano-Saucedo ORCID,Ana Cecilia Cepeda-Nieto ORCID,Maria Y Alvarado-Cervantes ORCID,Vianca Ibarra-Garcia ORCID,Daniel Barr ORCID

Live enrichment

PubMed:39759977 OpenAlex:https://openalex.org/W4405856655

National Institutes of Health

Grant: R56 [HL47678]

National Institutes of Health

Grant: R01 [HL152201]

FWCI

0.30

Citation Percentile

0.7%

Citation Trend

2026

goldLicense: cc-by

journalhttps://doi.org/10.1155/crig/9517735

publisherhttps://doi.org/10.1155/crig/9517735

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1155/crig/9517735

repositoryhttps://pubmed.ncbi.nlm.nih.gov/39759977

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/11699985

Fields of Study

Cardiomyopathy and Myosin StudiesCongenital heart defects researchNeurogenetic and Muscular Disorders Research

Keywords

MedicineDilated cardiomyopathyMutationCardiomyopathyInternal medicineCardiologyPediatricsGeneticsHeart failureGeneBiology

Sustainable Development Goals

SDG 0: Good health and well-being