Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene

American Journal of Ophthalmology

Volumn 124, Issue 1, 1997, Pages 95-102

  Andreasson, S ^a   Ponjavic, V ^a   Abrahamson, M ^a   Ehinger, B ^a   Wu, W ^a   Fujita, R ^a   Buraczynska, M ^a   Swaroop, A ^a  

^a LUND UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

GUANOSINE TRIPHOSPHATASE; MUTANT PROTEIN; REGULATOR PROTEIN;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DARK ADAPTATION; ELECTRORETINOGRAPHY; EXON; FAMILY; FEMALE; GENE DELETION; GENE MUTATION; HETEROZYGOTE; HUMAN; MALE; PEDIGREE; PERIMETRY; PHENOTYPE; PRIORITY JOURNAL; REGULATOR GENE; RETINITIS PIGMENTOSA; VISUAL IMPAIRMENT; X CHROMOSOME LINKAGE;

EID: 0030756190     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0002-9394(14)71649-6     Document Type: Article

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