Phenotypic Variability and Long-term Follow-up of Patients With Known and Novel PRPH2/RDS Gene Mutations

American Journal of Ophthalmology

Volumn 147, Issue 3, 2009, Pages

  Renner, Agnes B ^a,b   Fiebig, Britta S ^c   Weber, Bernhard H F ^c   Wissinger, Bernd ^d   Andreasson, Sten ^e   Gal, Andreas ^f   Cropp, Elke ^a   Kohl, Susanne ^d   Kellner, Ulrich ^a,g,h  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^b UNIVERSITY HOSPITAL REGENSBURG   (Germany)

^c UNIVERSITY OF REGENSBURG   (Germany)

^d Molekulargenetisches Labor   (Germany)

^e LUND UNIVERSITY HOSPITAL   (Sweden)

^f UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^g Augen Zentrum Siegburg   (Germany)

^h RetinaScience   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; PERIPHERIN;

ADULT; AMPLICON; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BLOOD SAMPLING; CLINICAL ARTICLE; CLINICAL EXAMINATION; DISEASE COURSE; DNA SEQUENCE; ELECTRORETINOGRAM; FAMILY STUDY; FEMALE; FLUORESCENCE ANGIOGRAPHY; GENE MUTATION; HUMAN; MALE; OPTICAL COHERENCE TOMOGRAPHY; PERIMETRY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RETINA CONE; RETINA DISEASE; RETINA MACULA AGE RELATED DEGENERATION; RETINA MACULA DEGENERATION; RETINA ROD; RETINITIS PIGMENTOSA; RETROSPECTIVE STUDY; VISION TEST;

EID: 59949102637     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ajo.2008.09.007     Document Type: Article

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