Retinopathy in Danon disease

Archives of Ophthalmology

Volumn 125, Issue 2, 2007, Pages 231-236

  Schorderet, Daniel F ^a,d   Cottet, Sandra ^a   Lobrinus, Johannes Alexander ^b   Borruat, François Xavier ^c   Balmer, Aubin ^c   Munier, Francis L ^c  

^a Institut de Recherche en Ophtalmologie   (Switzerland)

^b LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

^c HÔPITAL OPHTALMIQUE JULES GONIN   (Switzerland)

^d EPFL   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

LYSOSOME ASSOCIATED MEMBRANE PROTEIN 2;

ADULT; ARTICLE; CASE REPORT; CHILD; DANON DISEASE; ELECTRORETINOGRAPHY; EYE EXAMINATION; FAMILY HISTORY; FEMALE; FLUORESCENCE ANGIOGRAPHY; GENE EXPRESSION; GENE MUTATION; HEMIZYGOSITY; HETEROZYGOSITY; HETEROZYGOTE DETECTION; HUMAN; LINKAGE ANALYSIS; MALE; MICROSATELLITE MARKER; MUTATIONAL ANALYSIS; OPHTHALMOSCOPY; PATERNITY; PHENOTYPE; PRIORITY JOURNAL; RETINOPATHY; VISUAL ACUITY; X CHROMOSOME; X CHROMOSOME INACTIVATION;

ADOLESCENT; CHROMOSOMES, HUMAN, X; ELECTRORETINOGRAPHY; FEMALE; FLUORESCEIN ANGIOGRAPHY; GLYCOGEN STORAGE DISEASE TYPE IIB; HETEROZYGOTE; HUMANS; LINKAGE (GENETICS); LYSOSOME-ASSOCIATED MEMBRANE GLYCOPROTEINS; MALE; MICROSATELLITE REPEATS; MIDDLE AGED; MUTATION; PEDIGREE; PHENOTYPE; RETINAL DISEASES; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SIBLINGS; VISUAL ACUITY;

EID: 33846959828     PISSN: 00039950     EISSN: 00039950     Source Type: Journal    
DOI: 10.1001/archopht.125.2.231     Document Type: Article

References (18)

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