Clinical and oculomotor characteristics of albinism compared to FRMD7 associated infantile nystagmus

Investigative Ophthalmology and Visual Science

Volumn 52, Issue 5, 2011, Pages 2306-2313

  Kumar, Anil ^a   Gottlob, Irene ^a   Mclean, Rebecca J ^a   Thomas, Shery ^a   Thomas, Mervyn G ^a   Proudlock, Frank A ^a  

^a LEICESTER ROYAL INFIRMARY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ALBINISM; ARTICLE; CHILD; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE ASSOCIATION; EYE MOVEMENT; FRMD7 GENE; GENE; GENE MUTATION; HEAD POSITION; HUMAN; IDIOPATHIC INFANTILE NYSTAGMUS; INCIDENCE; MAJOR CLINICAL STUDY; NYSTAGMUS; PRESCHOOL CHILD; PRIORITY JOURNAL; RISK FACTOR; SCHOOL CHILD; STEREOSCOPIC VISION; STRABISMUS; WAVEFORM;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; ALBINISM, OCULAR; CHILD; CHILD, PRESCHOOL; CYTOSKELETAL PROTEINS; DEPTH PERCEPTION; ELECTRORETINOGRAPHY; EVOKED POTENTIALS, VISUAL; EYE MOVEMENTS; GENETIC DISEASES, X-LINKED; HUMANS; MEMBRANE PROTEINS; MIDDLE AGED; MUTATION; NYSTAGMUS, CONGENITAL; NYSTAGMUS, PATHOLOGIC; OCULOMOTOR MUSCLES; STRABISMUS; TOMOGRAPHY, OPTICAL COHERENCE;

EID: 79956039860     PISSN: 01460404     EISSN: 15525783     Source Type: Journal    
DOI: 10.1167/iovs.10-5685     Document Type: Article

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