Deletional mutations of dystrophin gene and carrier detection in eastern India

Indian Journal of Pediatrics

Volumn 76, Issue 10, 2009, Pages 1007-1012

  Basak, Jayasri ^a   Dasgupta, Uma B ^a   Mukherjee, Subhash Chandra ^b   Das, Shyamal Kumar ^c   Senapati, Asit Kumar ^c   Banerjee, Tapas Kumar ^d  

^a UNIVERSITY OF CALCUTTA   (India)

^b MEDICAL COLLEGE AND HOSPITAL   (India)

^c BANGUR INSTITUTE OF NEUROLOGY   (India)

^d PEERLESS HOSPITAL   (India)

Author keywords

Carrier identification; Deletion detection; DMD BMD; Eastern India; MPCR; Real time PCR

Indexed keywords

DYSTROPHIN;

ADOLESCENT; ARTICLE; BECKER MUSCULAR DYSTROPHY; CHILD; CONTROLLED STUDY; DIAGNOSTIC VALUE; DUCHENNE MUSCULAR DYSTROPHY; EXON; FAMILY; FEMALE; GENE AMPLIFICATION; GENE DELETION; GENE EXPRESSION; GENE FREQUENCY; GENE MUTATION; GENETIC COUNSELING; GENOTYPE; GERM LINE; HETEROZYGOTE DETECTION; HUMAN; INDIA; INFANT; MAJOR CLINICAL STUDY; MALE; MOSAICISM; MOTHER; MULTIPLEX POLYMERASE CHAIN REACTION; PHENOTYPE; PRESCHOOL CHILD; RADIOACTIVITY; REAL TIME POLYMERASE CHAIN REACTION; SCHOOL CHILD; SHORT TANDEM REPEAT;

ADOLESCENT; ADULT; AGE DISTRIBUTION; AGE OF ONSET; CHILD; CHILD, PRESCHOOL; CROSS-SECTIONAL STUDIES; DNA MUTATIONAL ANALYSIS; DYSTROPHIN; FEMALE; GENETICS, POPULATION; GERM-LINE MUTATION; HEALTH SURVEYS; HETEROZYGOTE; HUMANS; INCIDENCE; INDIA; MALE; MIDDLE AGED; MUSCULAR DYSTROPHY, DUCHENNE; POLYMERASE CHAIN REACTION; RISK ASSESSMENT; SEQUENCE DELETION; SEX DISTRIBUTION; YOUNG ADULT;

EID: 70849086143     PISSN: 00195456     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12098-009-0214-y     Document Type: Article

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