Dystrophin and the Retina

This publication has 36 references indexed in Scilit:

• Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutations
  Human Genetics, 1999
• Redefinition of Dystrophin Isoform Distribution in Mouse Tissue by RT-PCR Implies Role in Nonmuscle Manifestations of Duchenne Muscular Dystrophy
  Molecular Genetics and Metabolism, 1998
• Correlation between electroretinogram findings and molecular analysis in the Duchenne muscular dystrophy phenotype.
  British Journal of Ophthalmology, 1994
• Dystrophin expression in the human retina is required for normal function as defined by electroretinography
  Nature Genetics, 1993
• Membrane organization of the dystrophin-glycoprotein complex
  Cell, 1991
• Åland Island eye disease (Forsius‐Eriksson ocular albinism) and an Xp21 deletion in a patient with duchenne muscular dystrophy, glycerol kinase deficiency, and congenital adrenal hypoplasia
  American Journal of Medical Genetics, 1990
• A°land Island Eye Disease (Forsius-Eriksson Syndrome) Associated With Contiguous Deletion Syndrome at Xp21
  Archives of Ophthalmology (1950), 1989
• The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle
  Nature, 1988
• Dystrophin: The protein product of the duchenne muscular dystrophy locus
  Cell, 1987
• Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
  Cell, 1987