CYP1B1, MYOC, and LTBP2 mutations in primary congenital glaucoma patients in the United States

American Journal of Ophthalmology

Volumn 155, Issue 3, 2013, Pages 508-517.e5

  Lim, Sing Hui ^a,b   Tran Viet, Khanh Nhat ^b   Yanovitch, Tammy L ^b,c   Freedman, Sharon F ^c   Klemm, Thomas ^a   Call, Whitney ^b   Powell, Caldwell ^b   Ravichandran, Ajay ^b   Metlapally, Ravikanth ^b   Nading, Erica B ^c   Rozen, Steve ^a   Young, Terri L ^a,b,c  

^a NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

^b DUKE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c DUKE UNIVERSITY EYE CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P450 1B1; DNA; LATENT TRANSFORMING GROWTH FACTOR BETA BINDING PROTEIN; LATENT TRANSFORMING GROWTH FACTOR BETA BINDING PROTEIN 2; MYOCILIN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ALLELE; ARTICLE; CASE CONTROL STUDY; CLINICAL ARTICLE; CONGENITAL GLAUCOMA; CONTROLLED STUDY; DNA SCREENING; DNA SEQUENCE; EXOME; FAMILY STUDY; FEMALE; GENE IDENTIFICATION; GENE MUTATION; GENE SEGREGATION; GENETIC VARIABILITY; HETEROZYGOTE DETECTION; HOMOZYGOTE; HUMAN; MALE; MISSENSE MUTATION; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIMARY GLAUCOMA; PRIORITY JOURNAL; RETROSPECTIVE STUDY; SANGER SEQUENCING; SINGLE NUCLEOTIDE POLYMORPHISM; UNITED STATES; WHOLE EXOME SEQUENCING;

EID: 84873727111     PISSN: 00029394     EISSN: 18791891     Source Type: Journal    
DOI: 10.1016/j.ajo.2012.09.012     Document Type: Article

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