Whole dystrophin gene analysis by next-generation sequencing: a comprehensive genetic diagnosis of Duchenne and Becker muscular dystrophy.

Molecular genetics and genomics : MGG

Volumn 289, Issue 5, 2014, Pages 1013-1021

  Wang, Yan ^a   Yang, Yao ^b   Liu, Jing ^b   Chen, Xiao Chun ^b   Liu, Xin ^b   Wang, Chun Zhi ^b   He, Xi Yu ^b  

^a People' Republic of China   (China)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

DMD PROTEIN, HUMAN; DYSTROPHIN;

ARTICLE; CHILD; CHROMOSOME BREAKAGE; DUCHENNE MUSCULAR DYSTROPHY; GENE DELETION; GENE DUPLICATION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETICS; HIGH THROUGHPUT SEQUENCING; HUMAN; INFANT; MALE; MOLECULAR DIAGNOSIS; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD;

BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; CHROMOSOME BREAKPOINTS; DNA MUTATIONAL ANALYSIS; DYSTROPHIN; GENE DUPLICATION; GENETIC ASSOCIATION STUDIES; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; INFANT; MALE; MOLECULAR DIAGNOSTIC TECHNIQUES; MOLECULAR SEQUENCE DATA; MUSCULAR DYSTROPHY, DUCHENNE; POLYMORPHISM, GENETIC; SEQUENCE DELETION;

EID: 84910020266     PISSN: None     EISSN: 16174623     Source Type: Journal    
DOI: 10.1007/s00438-014-0847-z     Document Type: Article

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