Mutations in the human skeletal muscle chloride channel gene (CLCN1) associated with dominant and recessive myotonia congenita

Neurology

Volumn 47, Issue 4, 1996, Pages 993-998

  Zhang, J ^a   George Jr , A L ^c   Griggs, R C ^d   Fouad, G T ^a   Roberts, J ^a   Kwiecinski H ^e   Connolly, A M ^f   Ptacek L J ^a,b  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF UTAH   (United States)

^c VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^d UNIVERSITY OF ROCHESTER SCHOOL OF MEDICINE AND DENTISTRY   (United States)

^e MEDICAL UNIVERSITY OF WARSAW   (Poland)

^f WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE CHANNEL;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; BECKER MUSCULAR DYSTROPHY; CLINICAL ARTICLE; CONTROLLED STUDY; FAMILY STUDY; GENE MUTATION; GENETIC LINKAGE; HUMAN; MUSCLE WEAKNESS; MYOTONIA; PRIORITY JOURNAL; SKELETAL MUSCLE; THOMSEN DISEASE;

EID: 0029853212     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.47.4.993     Document Type: Article

References (23)

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