Retinal and optic disc atrophy associated with a CACNA1F mutation in a Japanese family

Archives of Ophthalmology

Volumn 121, Issue 7, 2003, Pages 1028-1033

  Nakamura, Makoto ^a   Ito, Sei ^b   Piao, Chang Hua ^b   Terasaki, Hiroko ^b   Miyake, Yozo ^b  

^a NAGOYA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL L TYPE; GENOMIC DNA;

ADULT; ANALYTIC METHOD; ARTICLE; ASIAN; BIOMICROSCOPY; BLOOD; CASE REPORT; CATARACT; CLINICAL FEATURE; DISEASE COURSE; DISEASE SEVERITY; DNA EXTRACTION; ELECTRORETINOGRAPHY; EXON; EYE FUNDUS; EYE PHOTOGRAPHY; FAMILIAL DISEASE; FOLLOW UP; GENE DELETION; GENE INSERTION; GENE MUTATION; GENE SEQUENCE; GENOMICS; HEREDITARY OPTIC ATROPHY; HUMAN; MALE; MEDICAL EXAMINATION; NIGHT VISION; OPHTHALMOSCOPY; PRIORITY JOURNAL; RETINA ATROPHY; RETINA CONE; RETINA DEGENERATION; RETINA ROD; SEQUENCE ANALYSIS; SIBLING; TREATMENT OUTCOME; VISION TEST; VISUAL ACUITY; VISUAL DISORDER;

AMINO ACID SEQUENCE; ATROPHY; BASE SEQUENCE; CALCIUM CHANNELS; CALCIUM CHANNELS, L-TYPE; DNA MUTATIONAL ANALYSIS; ELECTRORETINOGRAPHY; EYE DISEASES, HEREDITARY; HUMANS; JAPAN; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; OPTIC ATROPHY; PEDIGREE; POLYMERASE CHAIN REACTION; RETINA; RETINAL DISEASES; SEQUENCE DELETION; VISION DISORDERS; VISUAL FIELDS;

EID: 0037587692     PISSN: 00039950     EISSN: None     Source Type: Journal    
DOI: 10.1001/archopht.121.7.1028     Document Type: Article

References (21)

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