Work

Heterogeneity of nemaline myopathy cases with skeletal muscle α‐actin gene mutations

Year: 2004

Type: article

Study design: Observational Study

Source: Annals of Neurology

DOI: 10.1002/ana.20157

Authors: Pankaj B. Agrawal, Corinne D. Strickland, Charles Midgett, Ana Morales, Daniel E. Newburger, Melisa A. Poulos, Kinga K. Tomczak, Monique M. Ryan, Susan T. Iannaccone, Tom O. Crawford, Nigel G. Laing, Alan H. Beggs

Institutions: Boston Children's Hospital, Harvard University, Texas Scottish Rite Hospital for Children, Johns Hopkins University, Johns Hopkins Medicine, The University of Western Australia, Harry Perkins Institute of Medical Research, Queen Elizabeth II Medical Centre

Language: English

Topic: Muscle Physiology and Disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Institute of Arthritis and Musculoskeletal and Skin Diseases, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: Genes and Therapies for Centronuclear Myopathies, G5850420747, Intellectual and Developmental Disablities Research Center, G943165902

OpenAlex ID: W1981870699

FWCI: 2.721

Cites: 31

Cited by: 146

Related to: 10