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DELETIONS IN THE 5' REGION OF DYSTROPHIN AND RESULTING PHENOTYPES

Muntoni, F; Gobbi, P; Sewry, C; Sherratt, T; Taylor, J; Sandhu, SK; Abbs, S; Roberts, R; Hodgson, SV; Bobrow, M (1994) DELETIONS IN THE 5' REGION OF DYSTROPHIN AND RESULTING PHENOTYPES. JOURNAL OF MEDICAL GENETICS, 31 (11). 843 - 847 (5). ISSN 0022-2593 https://doi.org/10.1136/jmg.31.11.843
SGUL Authors: Hodgson, Shirley Victoria

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Item Type: Article
Additional Information: PubMed ID: 7853367
Keywords: Adolescent, Adult, Child, Child, Preschool, Chromosome Deletion, Chromosome Mapping, Dystrophin, Exons, Female, Humans, Infant, Male, Muscular Dystrophies, Phenotype, Reading Frames, Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, BECKER MUSCULAR-DYSTROPHY, SKELETAL-MUSCLE, FRAMESHIFT DELETION, MOLECULAR-BASIS, GENE DELETIONS, C-TERMINUS, DMD GENE, DUCHENNE, ANTIBODIES, PROTEIN
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Cell Sciences (INCCCS)
Journal or Publication Title: JOURNAL OF MEDICAL GENETICS
ISSN: 0022-2593
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Dates:
DateEvent
1 November 1994Published
Web of Science ID: WOS:A1994PQ12900005
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URI: http://openaccess.sgul.ac.uk/id/eprint/2503
Publisher's version: https://doi.org/10.1136/jmg.31.11.843

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