Characterization of the Ocular Phenotype of Duchenne and Becker Muscular Dystrophy

Purpose: Dystrophin, the Duchenne muscular dystrophy gene product, has been localized to the outer plexiform layer of normal human retina. The purpose of this study is to define completely the ocular phenotype associated with mutations at Xp21, the Duchenne muscular dystrophy gene locus. Methods: Tw...

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Veröffentlicht in:	Ophthalmology (Rochester, Minn.) Minn.), 1994-05, Vol.101 (5), p.856-865
Hauptverfasser:	Sigesmund, Dayle A., Weleber, Richard G., Pillers, De-Ann M., Westall, Carol A., Panton, Carole M., Powell, Berkley R., Héon, Elise, Murphey, William H., Musarella, Maria A., Ray, Peter N.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Biological and medical sciences Child Color Perception Depth Perception Diseases of striated muscles. Neuromuscular diseases DNA - analysis Electroretinography Female Fundus Oculi Humans Light Male Medical sciences Middle Aged Muscular Dystrophies - genetics Muscular Dystrophies - physiopathology Neurology Phenotype Refractive Errors - physiopathology Retina - physiopathology Vision, Binocular Visual Acuity
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