Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion.

Journal of medical genetics

Volumn 40, Issue 8, 2003, Pages

  Gualandi, F ^a   Trabanelli, C ^a   Rimessi, P ^a   Calzolari, E ^a   Toffolatti, L ^a   Patarnello, T ^a   Kunz, G ^a   Muntoni, F ^a   Ferlini, A ^a  

^a UNIVERSITY OF FERRARA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROPHIN; RNA; RNA, CIRCULAR;

ALTERNATIVE RNA SPLICING; ANIMAL; ARTICLE; CHEMISTRY; CLINICAL TRIAL; CONFORMATION; DUCHENNE MUSCULAR DYSTROPHY; EXON; GENE DELETION; GENE EXPRESSION REGULATION; GENETICS; HUMAN; MOLECULAR GENETICS; MOUSE; MULTICENTER STUDY; NUCLEOTIDE SEQUENCE; PHENOTYPE;

ALTERNATIVE SPLICING; ANIMALS; BASE SEQUENCE; DYSTROPHIN; EXONS; GENE DELETION; GENE EXPRESSION REGULATION; HUMANS; MICE; MOLECULAR SEQUENCE DATA; MUSCULAR DYSTROPHY, DUCHENNE; NUCLEIC ACID CONFORMATION; PHENOTYPE; READING FRAMES; RNA;

MLCS; MLOWN;

EID: 0142155623     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.40.8.e100     Document Type: Article

References (0)