Analyses of the presence of mutations in Dystrophin protein to predict their relative influences in the onset of Duchenne Muscular Dystrophy

Cellular Signalling

Volumn 26, Issue 12, 2014, Pages 2857-2864

  Bhattacharya, Simanti ^a   Das, Amit ^a   Dasgupta, Rakhi ^a   Bagchi, Angshuman ^a  

^a UNIVERSITY OF KALYANI   (India)

Author keywords

Duchenne Muscular Dystrophy; Dystrophin protein; Mode of DMD onset; Pathogenic mutations; Severity of mutations

Indexed keywords

ACTIN BINDING PROTEIN; CYSTEINE; DYSTROPHIN; SPECTRIN; ACTIN; PROTEIN BINDING;

ARTICLE; CARBOXY TERMINAL SEQUENCE; DISEASE COURSE; DISEASE SEVERITY; DMD GENE; DUCHENNE MUSCULAR DYSTROPHY; GENE; HUMAN; HYDROGEN BOND; HYDROPHOBICITY; MISSENSE MUTATION; MOLECULAR MECHANICS; NUCLEOTIDE SEQUENCE; PATHOGENESIS; POINT MUTATION; PROTEIN ANALYSIS; PROTEIN INTERACTION; PROTEIN STRUCTURE; SIGNAL TRANSDUCTION; AMINO ACID SEQUENCE; ANIMAL; CHEMISTRY; GENETIC DATABASE; GENETICS; METABOLISM; MOLECULAR GENETICS; MUTATION; PHYLOGENY; PROTEIN TERTIARY STRUCTURE;

ACTINS; AMINO ACID SEQUENCE; ANIMALS; CONSERVED SEQUENCE; DATABASES, GENETIC; DYSTROPHIN; HUMANS; MOLECULAR SEQUENCE DATA; MUSCULAR DYSTROPHY, DUCHENNE; MUTATION; PHYLOGENY; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; REPETITIVE SEQUENCES, AMINO ACID;

EID: 84907668961     PISSN: 08986568     EISSN: 18733913     Source Type: Journal    
DOI: 10.1016/j.cellsig.2014.09.006     Document Type: Article

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