Detection of COL4A5 gene mutations in Chinese patients with Alport's syndrome

Nephrology Dialysis Transplantation

Volumn 19, Issue 5, 2004, Pages 1123-1128

  Pan, Xiaoxia ^a   Yan, Jingyin ^a   Ren, Hong ^a   Zhang, Wen ^a   Shi, Hao ^a   Yu, Haijin ^a   Wang, Chaohui ^a   Hao, Cuilan ^a   Chen, Xiaonong ^a   Chen, Nan ^a  

^a SHANGHAI SECOND MEDICAL UNIVERSITY   (China)

Author keywords

Alport's syndrome; COL4A5 gene; Gene polymorphism; Type IV collagen

Indexed keywords

COLLAGEN TYPE 4; GUANINE; THYMINE;

ADULT; ALPORT SYNDROME; AMINO ACID SUBSTITUTION; ARTICLE; CHINESE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DENATURING GRADIENT GEL ELECTROPHORESIS; DNA SEQUENCE; DNA SPLICING; EXON; EYE DISEASE; FAMILY; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC CODE; GENETIC LINKAGE; GENETIC POLYMORPHISM; GLOMERULUS BASEMENT MEMBRANE; HEARING LOSS; HUMAN; INTRON; MALE; MISSENSE MUTATION; NONSENSE MUTATION; PATHOGENESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; STATISTICAL SIGNIFICANCE; X CHROMOSOME LINKED DISORDER;

CHINA; CHROMOSOMES, HUMAN, X; CODON, NONSENSE; COLLAGEN TYPE IV; EXONS; HUMANS; INTRONS; MUTATION; MUTATION, MISSENSE; NEPHRITIS, HEREDITARY; POLYMERASE CHAIN REACTION;

EID: 2442543272     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/gfh099     Document Type: Article

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