Immunohistochemical study of caveolin-3 in idiopathic hyperCKaemia [4]

Journal of Neurology Neurosurgery and Psychiatry

Volumn 74, Issue 4, 2003, Pages 547-548

  Capasso, M ^a   Lupo, S ^a   Di Muzio, A ^a   Uncini, A ^a,c   Servidei, S ^b  

^a UNIVERSITY OF CHIETI   (Italy)

^b CATHOLIC UNIVERSITY   (Italy)

^c Ospedale Clinicizzato SS Annunziata   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CAVEOLIN 3; CREATINE KINASE;

ADULT; CREATINE KINASE BLOOD LEVEL; FATIGUE; FEMALE; GENE MUTATION; HUMAN; IMMUNOHISTOCHEMISTRY; LETTER; MALE; MALIGNANT HYPERTHERMIA; MYALGIA; NEUROMUSCULAR DISEASE; PHENOTYPE; PRIORITY JOURNAL;

ADOLESCENT; ADULT; CAVEOLIN 3; CAVEOLINS; CHILD; CHILD, PRESCHOOL; CREATINE KINASE; FEMALE; HUMANS; MALE; MIDDLE AGED; MUSCLE, SKELETAL; NEUROMUSCULAR DISEASES; RISK FACTORS;

EID: 0037381188     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.74.4.547     Document Type: Letter

References (6)

1. Rowland LP, Willner J, Cerri C, et al. Approaches to the membrane theory of Duchenne muscular dystrophy. In: Angelini C, Danieli GA, Fontanari D, eds. Muscular dystrophy research: advances and new trends. Amsterdam: Excerpta Medica, 1980:3-13.
2. Merlini L, Carbone I, Capanni C, et al. Familial isolated hyperCKaemia associated with a new mutation in the caveolin-3 (CAV-3) gene. J Neurol Neurosurg Psychiatry 2002;73:65-7.
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6. Tateyama M, Aoki M, Nishino I, et al. Mutation in the caveolin-3 gene causes a peculiar form of distal myopathy. Neurology 2002;58:323-5.