Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder becker muscular dystrophy phenotype?

Human Molecular Genetics

Volumn 2, Issue 1, 1993, Pages 39-42

  Vainzof, M ^a   Takata, R I ^a   Passos bueno, M R ^a   Pavanello, R C M ^a   Zatz, M ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROPHIN;

ADOLESCENT; AMINO TERMINAL SEQUENCE; ARTICLE; BECKER MUSCULAR DYSTROPHY; CARBOXY TERMINAL SEQUENCE; CASE REPORT; CHILD; DELETION MUTANT; DISEASE COURSE; DISEASE SEVERITY; FEMALE; GENE MUTATION; HUMAN; IMMUNOBLOTTING; IMMUNOFLUORESCENCE; MALE; MOLECULAR WEIGHT; NORMAL HUMAN; PHENOTYPE; PROGNOSIS; PROTEIN ANALYSIS; PROTEIN DOMAIN; PROTEIN STRUCTURE;

ADOLESCENT; ALLELES; BLOTTING, WESTERN; CASE REPORT; CHILD, PRESCHOOL; DNA; DYSTROPHIN; FLUORESCENT ANTIBODY TECHNIQUE; HUMAN; MALE; MUSCLES; MUSCULAR DYSTROPHIES; PHENOTYPE; POLYMERASE CHAIN REACTION; PROGNOSIS; SEQUENCE DELETION; SUPPORT, NON-U.S. GOV'T; X CHROMOSOME;

EID: 0027401081     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/2.1.39     Document Type: Article

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