Automated sequence screening of the entire dystrophin cDNA in Duchenne dystrophy: Point mutation detection
Document Type
Journal Article
Publication Date
2006
Journal
American Journal of Medical Genetics Part B-Neuropsychiatric Genetics
Volume
141B
Issue
1
Inclusive Pages
44-50
APA Citation
Hamed, S., & Hoffman, E. (2006). Automated sequence screening of the entire dystrophin cDNA in Duchenne dystrophy: Point mutation detection. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 141B (1). Retrieved from https://hsrc.himmelfarb.gwu.edu/smhs_peds_facpubs/4407
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