Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12.

Kerrison, J B; Koenekoop, R K; Arnould, V J; Zee, D; Maumenee, I H

Kerrison, J B; Koenekoop, R K; Arnould, V J; Zee, D; Maumenee, I H.

Affiliation

Kerrison JB; Johns Hopkins Center for Hereditary Eye Diseases, Wilmer Ophthalmological Institute, Johns Hopkins Hospital, Baltimore, MD 21287-9237, USA. kerrison@welchlink.welch.jhu.edu

Am J Ophthalmol ; 125(1): 64-70, 1998 Jan.

Article in En | MEDLINE | ID: mdl-9437315

Subject(s)

Chromosomes, Human, Pair 6/genetics; Evoked Potentials, Visual; Genetic Linkage; Nystagmus, Pathologic/congenital; Nystagmus, Pathologic/pathology; Adult; Aged; Child, Preschool; Electronystagmography; Electroretinography; Eye Movements/physiology; Female; Humans; Male; Nerve Fibers/physiology; Nystagmus, Pathologic/genetics; Nystagmus, Pathologic/physiopathology; Ophthalmoscopy; Optic Nerve/physiology; Pedigree; Prospective Studies; Retina/physiopathology; Visual Acuity/physiology

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Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 6 / Nystagmus, Pathologic / Evoked Potentials, Visual / Genetic Linkage Type of study: Observational_studies Limits: Adult / Aged / Child, preschool / Female / Humans / Male Language: En Journal: Am J Ophthalmol Year: 1998 Document type: Article Affiliation country: United States

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