Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy.

Malhotra, S B; Hart, K A; Klamut, H J; Thomas, N S; Bodrug, S E; Burghes, A H; Bobrow, M; Harper, P S; Thompson, M W; Ray, P N

Malhotra, S B; Hart, K A; Klamut, H J; Thomas, N S; Bodrug, S E; Burghes, A H; Bobrow, M; Harper, P S; Thompson, M W; Ray, P N.

Affiliation

Malhotra SB; Genetics Department, Hospital for Sick Children, Toronto, Ontario, Canada.

Science ; 242(4879): 755-9, 1988 Nov 04.

Article in En | MEDLINE | ID: mdl-3055295

Subject(s)

Muscle Proteins/genetics; Muscular Dystrophies/genetics; X Chromosome; Base Sequence; Blotting, Southern; Chromosome Deletion; DNA Probes; Dystrophin; Exons; Genes; Humans; Mutation; Phenotype

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Collection: 01-internacional Database: MEDLINE Main subject: X Chromosome / Muscle Proteins / Muscular Dystrophies Type of study: Prognostic_studies Limits: Humans Language: En Journal: Science Year: 1988 Type: Article Affiliation country: Canada

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