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Heterozygous Cystic Fibrosis Transmembrane Regulator Gene Missense Variants Are Associated With Worse Cardiac Function in Patients With Duchenne Muscular Dystrophy

Journal of the American Heart Association(2020)10.1161/jaha.120.016799Source: DataRank Database

Heterozygous Cystic Fibrosis Transmembrane Regulator Gene Missense Variants Are Associated With Worse Cardiac Function in Patients With Duchenne Muscular Dystrophy is a research paper published in Journal of the American Heart Association (2020). On theSindex it has a DataRank of 0. It has been cited 3 times.

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Open Access3 citations

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Enrichment:Funding (3 grants)OA: goldTopics (39)IDs (PubMed)

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Accessible (1/2)

Open Access

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Reusable (0/3)

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Authors (8)

Yanqiu Shao,Faris Araj ORCID,Alpesh Amin ORCID,Benjamin Greenberg ORCID,Mark H. Drazner ORCID

Live enrichment

PubMed:33003980

NICHD NIH HHS

Grant: P50 HD087351

NICHD NIH HHS

Grant: U54 HD087351

NHLBI NIH HHS

Grant: R01 HL102478

goldLicense: cc-by-nc-nd

publisherhttps://www.ahajournals.org/doi/pdf/10.1161/JAHA.120.016799

publisherhttps://www.ahajournals.org/doi/full/10.1161/JAHA.120.016799

repositoryhttps://escholarship.org/uc/item/22w8q3td

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/7792368

Fields of Study

AdultCardiomyopathiesCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorDystrophinFemaleGenetic Predisposition to DiseaseHeart Function TestsHumansMagnetic Resonance Imaging, CineMaleMuscular Dystrophy, DuchenneMutation, MissenseNatriuretic Peptide, BrainPeptide FragmentsStroke VolumeVentricular Dysfunction, LeftExome Sequencing

MeSH Terms

Keywords

Duchene muscular dystrophy–associated cardiomyopathygenetic modifierwhole exome sequencing