Homozygous SPEG Mutation Is Associated With Isolated Dilated Cardiomyopathy

Journal article

Peer reviewed

Mohammed Almannai, Shiyu Luo, Eissa Faqeih, Fuad Almutairi, Qifei Li and Pankaj B Agrawal

Circulation. Genomic and precision medicine, Vol.14(2), pp.255-257

2021-04-03

PMCID: PMC8058307

PMID: 33794647

Abstract

Ventricular Function, Left

Humans

Child, Preschool

Male

Infant

Cardiomyopathy, Dilated

Homozygote

Muscle Proteins

Mitral Valve Insufficiency

Gene Deletion

Adolescent

Protein Serine-Threonine Kinases

Electrocardiography

Female

Clinical Letter

Child

Infant, Newborn

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Collaboration types: Domestic collaboration; International collaboration
Citation topics: 1 Clinical & Life Sciences; 1.79 Molecular & Cell Biology - Physiology; 1.79.682 Sarcoplasmic Reticulum
Web Of Science research areas: Cardiac & Cardiovascular Systems; Genetics & Heredity
ESI research areas: Molecular Biology & Genetics

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Source: InCites

Title: Homozygous SPEG Mutation Is Associated With Isolated Dilated Cardiomyopathy
Creators: Mohammed Almannai
Shiyu Luo
Eissa Faqeih
Fuad Almutairi
Qifei Li
Pankaj B Agrawal
Publication Details: Circulation. Genomic and precision medicine, Vol.14(2), pp.255-257
Publisher: Lippincott Williams & Wilkins
Number of pages: 3
Grant note: R01 AR068429 / National Institute of Arthritis and Musculoskeletal and Skin Diseases of National Institute of Health (NIH)
Academic Unit: Miller School of Medicine; UMMG Dept of Pediatrics - Neonatology; UMMG Department of Pediatrics
Language: English
Resource Type: Journal article
PMID: 33794647
PMCID: PMC8058307
Record Identifier: 991031970902102976