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Ophthalmic Genetics

Volumn 22, Issue 3, 2001, Pages 187-194

Novel deletion of the RPGR gene in a Chinese family with X-linked retinitis pigmentosa

(6) Zhao, Kanxing a Wang, Lejin a Wang, Li a Wang, Liming a Zhang, Qingsheng a Wang, Qing a

a LERNER RESEARCH INSTITUTE (United States)

Author keywords

Genetic disease; Retinal degeneration; Retinal dystrophy; Retinitis pigmentosa; RP3; RPGR; X linked

Indexed keywords

PROTEIN DERIVATIVE; PROTEIN RPGR; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CARBOXY TERMINAL SEQUENCE; CHINESE; CLINICAL ARTICLE; CONTROLLED STUDY; DNA POLYMORPHISM; DNA SEQUENCE; ELECTRORETINOGRAM; EXON; FAMILY STUDY; FEMALE; GENE DELETION; GENE IDENTIFICATION; GENE LOCUS; GENE MAPPING; GENE MUTATION; HAPLOTYPE; HETEROZYGOTE; HUMAN; MALE; MARKER GENE; MYOPIA; PEDIGREE; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; SINGLE STRAND CONFORMATION POLYMORPHISM; STOP CODON; X CHROMOSOME LINKAGE;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; BASE SEQUENCE; CARRIER PROTEINS; CHINA; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; EYE PROTEINS; FEMALE; FLUORESCEIN ANGIOGRAPHY; GENE DELETION; HUMANS; LINKAGE (GENETICS); MALE; MICROSATELLITE REPEATS; MIDDLE AGED; MOLECULAR SEQUENCE DATA; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RETINA; RETINITIS PIGMENTOSA; X CHROMOSOME;

EID: 0035572954 PISSN: 13816810 EISSN: None Source Type: Journal
DOI: 10.1076/opge.22.3.187.2221 Document Type: Article

Times cited : (10)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.