Small mutations detected by multiplex ligation-dependent probe amplification of the dystrophin gene.

Genetic testing and molecular biomarkers

Volumn 13, Issue 3, 2009, Pages 427-431

  Okizuka, Y ^a   Takeshima, Yasuhiro ^a   Awano, Hiroyuki ^a   Zhang, Zhujun ^a   Yagi, Mariko ^a   Matsuo, Masafumi ^a  

^a KOBE UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROPHIN; PRIMER DNA;

ARTICLE; ASIAN; DUCHENNE MUSCULAR DYSTROPHY; EXON; GENE DELETION; GENE DUPLICATION; GENETICS; HUMAN; MALE; METHODOLOGY; MUTATION; NUCLEIC ACID AMPLIFICATION; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; STOP CODON;

ASIAN CONTINENTAL ANCESTRY GROUP; CODON, NONSENSE; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; DYSTROPHIN; EXONS; GENE DUPLICATION; HUMANS; MALE; MUSCULAR DYSTROPHY, DUCHENNE; MUTATION; NUCLEIC ACID AMPLIFICATION TECHNIQUES; POLYMERASE CHAIN REACTION; SEQUENCE DELETION;

EID: 67651071695     PISSN: None     EISSN: 19450257     Source Type: Journal    
DOI: 10.1089/gtmb.2009.0002     Document Type: Article

References (0)