Myopathy as the first symptom of hypokalemic periodic paralysis--case report of a girl from a Polish family with CACNA1S (R1239G) mutation.

Advances in medical sciences

Volumn 52 Suppl 1, Issue , 2007, Pages 155-157

  Winczewska Wiktor, A ^a   Steinborn, B ^a   Lehman Horn, F ^a   Biczysko, W ^a   Wiktor, M ^a   Gurda, B ^a   Jurkat Rott, K ^a  

^a POZNAN UNIVERSITY OF MEDICAL SCIENCES   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

CACNA1S PROTEIN, HUMAN; CALCIUM CHANNEL; UNCLASSIFIED DRUG;

ADOLESCENT; ARTICLE; CASE REPORT; CHILD; FEMALE; GENETICS; HUMAN; MALE; MUTATION; ONSET AGE; PEDIGREE; PERIODIC PARALYSIS; PRESCHOOL CHILD;

ADOLESCENT; AGE OF ONSET; CALCIUM CHANNELS; CHILD; CHILD, PRESCHOOL; FEMALE; HUMANS; MALE; MUTATION; PARALYSIS, HYPERKALEMIC PERIODIC; PEDIGREE;

EID: 40049098181     PISSN: 18961126     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)