A common NYX mutation in Flemish patients with X linked CSNB

British Journal of Ophthalmology

Volumn 93, Issue 5, 2009, Pages 692-696

  Leroy, B P ^a   Budde, B S ^b   Wittmer, M ^c   De Baere, E ^a   Berger, W ^c   Zeitz, C ^c,d  

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

^b UNIVERSITY OF COLOGNE   (Germany)

^c UNIVERSITY OF ZURICH   (Switzerland)

^d INSTITUT DE LA VISION   (France)

Author keywords

[No Author keywords available]

Indexed keywords

METABOTROPIC RECEPTOR 6; NYCTALOPIN; PROTEIN SERINE KINASE; UNCLASSIFIED DRUG; NYX PROTEIN, HUMAN; PROTEOGLYCAN;

ARTICLE; AUTOFLUORESCENCE; CLINICAL ARTICLE; CONGENITAL STATIONARY NIGHT BLINDNESS; CONTROLLED STUDY; FRAMESHIFT MUTATION; GENE DELETION; HAPLOTYPE; HUMAN; MALE; NIGHT BLINDNESS; OPHTHALMOSCOPY; PEDIGREE ANALYSIS; PRIORITY JOURNAL; STOP CODON; UNTRANSLATED REGION; ADOLESCENT; ADULT; ELECTRORETINOGRAPHY; FEMALE; GENETICS; GENOTYPE; HETEROZYGOTE; METHODOLOGY; MUTATION; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; PEDIGREE; X CHROMOSOME LINKED DISORDER;

ADOLESCENT; ADULT; DNA MUTATIONAL ANALYSIS; ELECTRORETINOGRAPHY; FEMALE; GENETIC DISEASES, X-LINKED; GENOTYPE; HAPLOTYPES; HETEROZYGOTE; HUMANS; MALE; MUTATION; NIGHT BLINDNESS; PEDIGREE; PROTEOGLYCANS;

EID: 66149116906     PISSN: 00071161     EISSN: 14682079     Source Type: Journal    
DOI: 10.1136/bjo.2008.143727     Document Type: Article

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