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Volumn 21, Issue 3, 2000, Pages 191-193

Novel compound hoterozygous mutations in the cytochrome P4501B1 gene (CYP1B1) in a Japanese patient with primary congenital glaucoma

Author keywords

Congenital glaucoma; CYP1B1; Cytochrome P4501B1; Mutation

Indexed keywords

CYTOCHROME P450; CYTOCHROME P450 1B1; UNCLASSIFIED DRUG; CYTOCHROME P 450 CYP1B1; CYTOCHROME P-450 CYP1B1; PRIMER DNA; UNSPECIFIC MONOOXYGENASE;

EID: 0033623590     PISSN: 13816810     EISSN: None     Source Type: Journal    
DOI: 10.1076/1381-6810(200009)21:3;1-z;ft191     Document Type: Article
Times cited : (18)

References (9)
  • 6
    • 0030942553 scopus 로고    scopus 로고
    • Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal Cause of primary congenital glaucoma (buphthalmos) in families linked to the GLC3A locus on chromosome 2p21
    • (1997) Hum Mol Genet , vol.6 , pp. 641-647
    • Stoilov, I.1    Akarsu, A.N.2    Sarfarazi, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.