Facioscapulohumeral muscular dystrophy. The spectrum of clinical manifestations and molecular genetic changes;Fazioskapulohumerale muskeldystrophie. Spektrum der klinischen manifestationen und molekulargenetischen veränderungen

Nervenarzt

Volumn 74, Issue 2, 2003, Pages 151-158

  Krasnianski, M ^a   Neudecker, S ^a   Eger, K ^a   Schulte Mattler, W ^a   Zierz, S ^a  

^a MARTIN LUTHER UNIVERSITY HALLE WITTENBERG   (Germany)

Author keywords

Facioscapulohumeral muscular dystrophy; Progressive muscular dystrophy

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE MARKER; FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FEMALE; GENE DELETION; GENETIC PREDISPOSITION; HUMAN; MALE; PHENOTYPE;

ADOLESCENT; ADULT; AGED; BIOPSY; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 4; ELECTROMYOGRAPHY; FEMALE; GENOTYPE; HUMANS; MALE; MIDDLE AGED; MUSCLE, SKELETAL; MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL; NEUROLOGIC EXAMINATION; PHENOTYPE;

EID: 0038813973     PISSN: 00282804     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00115-002-1455-4     Document Type: Article

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