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
Related URLs:	Author
Dates:	Date Event 1 November 1994 Published
Web of Science ID:	WOS:A1994PQ12900005
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URI:	https://openaccess.sgul.ac.uk/id/eprint/2503
Publisher's version:	https://doi.org/10.1136/jmg.31.11.843

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