Autosomal dominant retinitis pigmentosa in a five-generation pedigree in People's Republic of China [3]

Eye

Volumn 17, Issue 9, 2003, Pages 1036-1039

  Teng, Y ^a   Wang, W ^a,b,c   Tian, H ^a   Wang, H ^a   Hu, X ^a   Chen, Y ^a   Bittles, A H ^b  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b EDITH COWAN UNIVERSITY   (Australia)

^c PEKING UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ASTIGMATISM; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHILD; CHINA; CHROMOSOME ABERRATION; CONTROLLED STUDY; DNA SEQUENCE; DOMINANT GENE; FEMALE; GENE MAPPING; GENE MUTATION; GENETIC HETEROGENEITY; GENETICS; HUMAN; LETTER; MAJOR CLINICAL STUDY; MALE; MUTATION; MYOPIA; NIGHT BLINDNESS; OPHTHALMOSCOPY; PEDIGREE; PEDIGREE ANALYSIS; PRESCHOOL CHILD; PREVALENCE; RETINITIS PIGMENTOSA; VISUAL FIELD DEFECT; VISUAL IMPAIRMENT;

EID: 0346327156     PISSN: 0950222X     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.eye.6700499     Document Type: Letter

References (9)

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