SCOPUS 정보 검색 플랫폼

Volumn 70, Issue 4, 2002, Pages 1049-1053

X-linked cone-rod dystrophy (Locus COD1): Identification of mutations in RPGR exon ORF15

(10) Demirci, F Yesim K a,b Rigatti, Brian W a Wen, Gaiping c Radak, Amy L b Mah, Tammy S a,b Baic, Corrine L a Traboulsi, Elias I d Alitalo, Tiina e Ramser, Juliane f Gorin, Michael B a,b

a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE (United States)

b UNIVERSITY OF PITTSBURGH (United States)

c FRITZ LIPMANN INSTITUTE (Germany)

d LERNER RESEARCH INSTITUTE (United States)

e HELSINKI UNIVERSITY CENTRAL HOSPITAL (Finland)

f UNIVERSITY OF MUNICH (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ELECTRORETINOGRAPHY; EXON; FRAMESHIFT MUTATION; GENE DELETION; GENE INSERTION; GENE MUTATION; GENETIC RECOMBINATION; HUMAN; NUCLEOTIDE SEQUENCE; PENETRANCE; PHOTORECEPTOR; PRIORITY JOURNAL; RETINA CONE; RETINA DEGENERATION; RETINA DYSTROPHY; RETINA ROD; X CHROMOSOME LINKAGE;

INSERTION SEQUENCES;

EID: 0036204904 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: 10.1086/339620 Document Type: Article

Times cited : (147)

References (25)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.