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Volumn 32, Issue 7-8, 2007, Pages 685-691

Identification of novel mutations in the XLRS1 gene in Chinese patients with X-linked juvenile retinoschisis

Author keywords

Frameshift; Missense mutations; XLRS; XLRS1 gene

Indexed keywords

ARTICLE; CHILD; CHINESE; CLINICAL ARTICLE; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; EXON; FRAMESHIFT MUTATION; GENE; GENE DELETION; GENE IDENTIFICATION; GENETIC ASSOCIATION; HETEROZYGOTE; HUMAN; MALE; MISSENSE MUTATION; PEDIGREE ANALYSIS; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; PROGENY; RETINOSCHISIS; SINGLE STRAND CONFORMATION POLYMORPHISM; X CHROMOSOME LINKED DISORDER; XLRS1 GENE;

EID: 34548660425     PISSN: 02713683     EISSN: 14602202     Source Type: Journal    
DOI: 10.1080/02713680701486410     Document Type: Article
Times cited : (5)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.