Point mutation in the human dystrophin gene: Identification through Western blot analysis-Reference-Cited by-同舟云学术

Point mutation in the human dystrophin gene: Identification through Western blot analysis

Published:1991-06 Issue:2 Volume:10 Page:457-460
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Bulman Dennis E.,Gangopadhyay Suman B.,Bebchuck Karen G.,Worton Ronald G.,Ray Peter N.

Publisher

Elsevier BV

Subject

Genetics

Reference24 articles.

1. Differentiation of Duchenne and Becker muscular dystrophy with amino- and carboxy-terminal antisera specific for dystrophin;Bulman;Am. J. Hum. Genet,1991

2. Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification;Chamberlain;Nucleic Acids Res,1988

3. Single step method of RNA isolation by acid guanidinium thiocyanatephenol-chloroform extraction;Chomczynski;Anal. Biochem,1987

4. α-Actinin and the DMD protein containing spectrin-like repeats;Davison;Cell,1988

5. Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels;Den Dunnen;Nature,1987

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