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Volumn 24, Issue 3, 2001, Pages 340-344

Rippling muscle disease: Evidence for phenotypic and genetic heterogeneity

Author keywords

Contracture; Muscle cramps; Myopathy; Myotonia; Rippling muscle disease

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CATTLE; CHROMOSOME 1Q; CLINICAL ARTICLE; CLINICAL FEATURE; FAMILY STUDY; FEMALE; GENETIC HETEROGENEITY; GENETIC LINKAGE; HUMAN; MALE; MUSCLE CONTRACTION; MUSCLE DISEASE; MUSCLE STIFFNESS; MYALGIA; MYOTONIA; PHENOTYPE; PRIORITY JOURNAL;

EID: 0035117623     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1097-4598(200103)24:3<340::AID-MUS1003>3.0.CO;2-X     Document Type: Article
Times cited : (30)

References (14)
  • 5
    • 0024495634 scopus 로고
    • Hereditary increased muscle mechanical irritability and progressive contracture with stretch-induced electromyographic activity
    • (1989) Muscle Nerve , vol.12 , pp. 103-107
    • Jusic, A.1
  • 12
    • 0016693399 scopus 로고
    • A family with dominant hereditary myotonia, muscular hypertrophy, and increased muscular irritability, distinct from myotonia congenita Thomsen
    • (1975) Acta Neurol Scand , vol.51 , pp. 225-232
    • Torbergsen, T.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.