Variants of RP1 gene in Chinese patients with autosomal dominant retinitis pigmentosa

Canadian Journal of Ophthalmology

Volumn 43, Issue 2, 2008, Pages 208-212

  Sheng, Xunlun ^a,b   Zhang, Xinfang ^a   Wu, Weimin ^a   Zhuang, Wenjuan ^a   Meng, Ruihua ^c   Rong, Weining ^a  

^a NINGXIA MEDICAL UNIVERSITY   (China)

^b The First People's Hospital of Qingdao Economic and Technological Development Zone   (China)

^c QINGDAO UNIVERSITY MEDICAL COLLEGE   (China)

Author keywords

Causative mutation; Retinitis pigmentosa; RP1 gene

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE COURSE; DNA POLYMORPHISM; DNA SEQUENCE; EYE EXAMINATION; FEMALE; GENE; GENE MUTATION; HUMAN; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; RETINITIS PIGMENTOSA; RNA SPLICING; RP1 GENE;

EID: 42049105967     PISSN: 00084182     EISSN: 17153360     Source Type: Journal    
DOI: 10.3129/I08-004     Document Type: Article

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