DNA linkage based diagnosis of Wilson disease in asymptomatic siblings

Indian Journal of Medical Research

Volumn 118, Issue NOV., 2003, Pages 208-214

  Gupta, A ^a   Neogi, R ^a   Mukherjea, M ^b   Mukhopadhyay, A ^a   Roychoudhury, S ^a   Senapati, A ^c   Gangopadhyay, P K ^c   Ray, Kunal ^a  

^a INDIAN INSTITUTE OF CHEMICAL BIOLOGY   (India)

^b TUFTS UNIVERSITY   (United States)

^c BANGUR INSTITUTE OF NEUROLOGY   (India)

Author keywords

ATP7B; Genotype; Haplotype; Microsatellite; Wilson disease

Indexed keywords

CERULOPLASMIN; COPPER; DNA FRAGMENT; GENOMIC DNA; PENICILLAMINE; ZINC;

ADOLESCENT; ADULT; ALLELE; ARTICLE; CHILD; COMPUTER PROGRAM; DIAGNOSTIC PROCEDURE; DINUCLEOTIDE REPEAT; DNA FLANKING REGION; DNA SEQUENCE; FEMALE; FLUORESCENCE ANALYSIS; GENE AMPLIFICATION; GENE LOCUS; GENE MUTATION; GENE SEGREGATION; GENETIC HETEROGENEITY; GENETIC MARKER; GENOTYPE; HAPLOTYPE; HUMAN; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MALE; PARENT; POLYACRYLAMIDE GEL ELECTROPHORESIS; POLYMERASE CHAIN REACTION; RELATIVE; SEGREGATION ANALYSIS; SEQUENCE ANALYSIS; SIBLING; SYMPTOM; URINARY EXCRETION; WILSON DISEASE;

ADOLESCENT; FEMALE; GENETIC SCREENING; HEPATOLENTICULAR DEGENERATION; HUMANS; LINKAGE (GENETICS); MALE; PEDIGREE; SIBLINGS;

EID: 0347917313     PISSN: 09715916     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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