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Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V

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Year: 2003
Type: article
Study design: Observational Study
Source: The American Journal of Human Genetics
DOI: 10.1086/375039
Authors: Anthony Antonellis, Rachel E. Ellsworth, Nyamkhishig Sambuughin, Imke Puls, Annette Abel, Shih-Queen Lee-Lin, Albena Jordanova, Ivo Kremensky, Kyproula Christodoulou, Lefkos T. Middleton, Kumaraswamy Sivakumar, Victor Ionasescu, Benoit Funalot, Jeffery M. Vance, Lev G. Goldfarb, Kenneth H. Fischbeck, Eric D. Green
Institutions: National Institutes of Health, George Washington University, National Human Genome Research Institute, Barrow Neurological Institute, Medical University of Sofia, Cyprus Institute of Neurology and Genetics, University of Iowa, Inserm, Centre Hospitalier Sainte-Anne, Duke University, National Institute of Neurological Disorders and Stroke
Language: English

Topic: Hereditary Neurological Disorders
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: bronze

Funder: National Institute of Neurological Disorders and Stroke
Award: Genetic Studies in Neurological Disorders
OpenAlex ID: W2040724884
FWCI: 8.314
Cites: 16
Cited by: 582
Related to: 10
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