CRYBB1 mutation associated with congenital cataract and microcornea

Molecular Vision

Volumn 11, Issue , 2005, Pages 587-593

  Willoughby, Colin E ^a,b   Shafiq, Ayad ^c   Ferrini, Walter ^a   Chan, Louie Loh Yen ^a   Billingsley, Gail ^a   Priston, Megan ^a   Mok, Calvin ^a   Chandna, Arvind ^d   Kaye, Stephen ^e   Héon, Elise ^a  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b QUEEN'S UNIVERSITY BELFAST   (United Kingdom)

^c ROYAL VICTORIA INFIRMARY   (United Kingdom)

^d ALDER HEY CHILDREN S HOSPITAL   (United Kingdom)

^e ROYAL LIVERPOOL UNIVERSITY HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BETA CRYSTALLIN;

ADOLESCENT; ADULT; AGED; ARTICLE; CATARACT EXTRACTION; CATARACTOGENESIS; CHILD; CHROMOSOME 22Q; CLINICAL ARTICLE; CONGENITAL CATARACT; CONTROLLED STUDY; CORNEA DISEASE; CORNEA SURGERY; DNA FLANKING REGION; EXON; FAMILY HISTORY; GENE AMPLIFICATION; GENE CLUSTER; GENE MUTATION; GENE SEQUENCE; HETEROZYGOSITY; HUMAN; INFANT; INTRON; MICROSATELLITE MARKER; NUCLEOTIDE SEQUENCE; PHENOTYPE; POLYMERASE CHAIN REACTION; PREDICTION; PRIORITY JOURNAL; PROTEIN INTERACTION; SINGLE STRAND CONFORMATION POLYMORPHISM; UNITED KINGDOM;

ADOLESCENT; ADULT; AGED; BETA-CRYSTALLIN B CHAIN; CATARACT; CHILD; CHROMOSOMES, HUMAN, PAIR 22; CORNEA; DNA MUTATIONAL ANALYSIS; EYE ABNORMALITIES; FEMALE; GENES, DOMINANT; HUMANS; INFANT; LINKAGE (GENETICS); MALE; MIDDLE AGED; MUTATION; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 26244461031     PISSN: 10900535     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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