Work

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

Year: 1987

Type: article

Study design: Observational Study

Source: Cell

DOI: 10.1016/0092-8674(87)90504-6

Authors: M. Koenig, E.P. Hoffman, C.J. Bertelson, A.P. Monaco, C. Feener, L.M. Kunkel

Institutions: Boston Children's Hospital, Harvard University, Howard Hughes Medical Institute

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: Muscular Dystrophy Association, National Institutes of Health, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G3446264458, Medical Scientist Training Program, G4360979880, G573904840, DYSTROPHIN AND RELATED PROTEINS IN NEUROMUSCULAR DISEASE, G689141124

OpenAlex ID: W2018600945

FWCI: 43.52

Cites: 45

Cited by: 2,399

Related to: 10