Cerulean cataract mapped to 12q13 and associated with a novel initiation codon mutation in MIP

Molecular Vision

Volumn 17, Issue , 2011, Pages 2049-2055

  Xiao, Xueshan ^a   Li, Wei ^b   Wang, Panfeng ^a   Li, Lin ^a   Li, Shiqiang ^a   Jia, Xiaoyun ^a   Sun, Wenmin ^a   Guo, Xiangming ^a   Zhang, Qingjiong ^a  

^a SUN YAT SEN UNIVERSITY   (China)

^b Shenzhen Second Hospital   (China)

Author keywords

[No Author keywords available]

Indexed keywords

BETA CRYSTALLIN; GAMMA CRYSTALLIN; GENOMIC DNA;

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CERULEAN CATARACT; CHILD; CHINESE; CHROMOSOME 12Q; CHROMOSOME MAP; CLINICAL ARTICLE; CODON; CONGENITAL CATARACT; CONTROLLED STUDY; CRYBB2 GENE; CRYGD GENE; DISEASE ASSOCIATION; FAMILY STUDY; FEMALE; GENE; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; HETEROZYGOTE; HUMAN; LINKAGE ANALYSIS; MAF GENE; MALE; MIP GENE; PRIORITY JOURNAL; SCHOOL CHILD; TRANSLATION INITIATION;

AQUAPORINS; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CASE-CONTROL STUDIES; CATARACT; CHROMOSOMES, HUMAN, PAIR 12; CODON, INITIATOR; DNA MUTATIONAL ANALYSIS; EYE PROTEINS; FEMALE; GENES, DOMINANT; GENETIC LINKAGE; GENOME-WIDE ASSOCIATION STUDY; HAPLOTYPES; HETEROZYGOTE; HUMANS; LENS, CRYSTALLINE; LOD SCORE; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE;

EID: 79961239596     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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