Becker muscular dystrophy combined with X-linked Charcot-Marie-Tooth neuropathy

Muscle and Nerve

Volumn 23, Issue 5, 2000, Pages 818-823

  Bergmann, Carsten ^a   Senderek, Jan ^a   Hermanns, Benita ^a   Jauch, Anna ^b   Janssen, Bart ^b   Schröder, J Michael ^a   Karch, Dieter ^c  

^a RWTH AACHEN UNIVERSITY   (Germany)

^b UNIVERSITY OF HEIDELBERG   (Germany)

^c Sozialpädiatre Kinderzentrum   (Germany)

Author keywords

Charcot Marie Tooth neuropathy; Duchenne Becker muscular dystrophy; Hereditary motor and sensory neuropathy; Muscular dystrophy; X linked

Indexed keywords

ARGININE; CONNEXIN 32; CREATINE KINASE; DNA; DYSTROPHIN; TRYPTOPHAN;

ADULT; AGAR GEL ELECTROPHORESIS; ARTICLE; BECKER MUSCULAR DYSTROPHY; CASE REPORT; ELECTROMYOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN TISSUE; MALE; MUSCLE BIOPSY; NERVE CONDUCTION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SOUTHERN BLOTTING; X CHROMOSOME;

ADULT; CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; CONNEXINS; DISEASE PROGRESSION; FEMALE; GENOMIC IMPRINTING; HUMANS; MALE; MUSCULAR DYSTROPHY, DUCHENNE; PEDIGREE; X CHROMOSOME;

EID: 0034023968     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-4598(200005)23:5<818::AID-MUS23>3.0.CO;2-O     Document Type: Article

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