The RPGRIP1-related retinal phenotype in children

British Journal of Ophthalmology

Volumn 97, Issue 6, 2013, Pages 760-764

  Khan, Arif O ^a,b   Abu Safieh, Leen ^b   Eisenberger, Tobias ^c   Bolz, Hanno J ^c,d   Alkuraya, Fowzan S ^a,e,f  

^a KING KHALED EYE SPECIALIST HOSPITAL   (Saudi Arabia)

^b KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

^c Center for Human Genetics   (Germany)

^d UNIVERSITY OF COLOGNE   (Germany)

^e KING KHALID UNIVERSITY HOSPITAL   (Saudi Arabia)

^f ALFAISAL UNIVERSITY   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOFLUORESCENCE; CHILD; CLINICAL ARTICLE; CONVERGENT STRABISMUS; DAY BLINDNESS; ELECTRORETINOGRAPHY; FEMALE; GENE; GENE MUTATION; HOMOZYGOSITY; HUMAN; LEBER CONGENITAL AMAUROSIS; MALE; NYSTAGMUS; PHENOTYPE; PHOTOPHOBIA; PIGMENT EPITHELIUM; PRESCHOOL CHILD; PRIORITY JOURNAL; RETROSPECTIVE STUDY; RPGRIP1 GENE; SCHOOL CHILD; STRABISMUS;

CHILD HEALTH (PAEDIATRICS); ELECTROPHYSIOLOGY; GENETICS; RETINA;

CHILD; CHILD, PRESCHOOL; EYEGLASSES; FEMALE; GENES, RECESSIVE; HUMANS; LEBER CONGENITAL AMAUROSIS; MALE; OPHTHALMOSCOPY; PHENOTYPE; PROTEINS; REFRACTIVE ERRORS; RETINAL DYSTROPHIES; RETINITIS PIGMENTOSA; RETROSPECTIVE STUDIES;

EID: 84878011304     PISSN: 00071161     EISSN: 14682079     Source Type: Journal    
DOI: 10.1136/bjophthalmol-2012-303050     Document Type: Article

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