Immunofluorescence dystrophin study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal region of the protein

Author:

Vainzof M.,Zubrzycka-Gaarn E.E.,Rapaport D.,Passos-Bueno M.R.,Pavanello R.C.M.,Pavanello-Filho I.,Zatz M.

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference32 articles.

1. Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide;Arahata;Nature,1988

2. Duchenne muscular dystrophy: Deficiency of dystrophin at the muscle cell surface;Bonilla;Cell,1988

3. Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: Location of break points on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutation;Darras;Am. J. Hum. Genet.,1988

4. Very mild muscular dystrophy associated with the deletion of 46% of dystrophin;England;Nature,1990

5. Preferential detection of exons in Duchenne and Becker muscular dystrophies;Forrest;Nature,1987

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