Paramyotonia congenita: Genotype to phenotype correlations in two families and report of a new mutation in the sodium channel gene

Journal of the Neurological Sciences

Volumn 142, Issue 1-2, 1996, Pages 126-133

  Plassart, E ^a   Eymard, B ^a   Maurs, L ^a   Hauw, J J ^a   Lyon Caen, O ^a   Fardeau, M ^a   Fontaine, B ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

genotype to phenotype correlation; hyperkalemic periodic paralysis; mutation; paramyotonia congenita; sodium channel

Indexed keywords

SODIUM CHANNEL;

ADOLESCENT; ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FAMILIAL DISEASE; FEMALE; HUMAN; MALE; MOLECULAR BIOLOGY; MUTATION; PRIORITY JOURNAL; SCHOOL CHILD; THOMSEN DISEASE;

EID: 0030271970     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0022-510X(96)00173-6     Document Type: Article

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