Literature DB >> 10881598

Hypokalemic periodic paralysis and mutations in the CACNL1A3 gene: case study in a Japanese family.

T Wada1, A Yachie, S Fujita, K Takei, R Sumita, T Ichihara, S Koizumi.   

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Year:  2000        PMID： 10881598     DOI： 10.1046/j.1442-200x.2000.01214.x

Source DB:  PubMed          Journal:  Pediatr Int        ISSN： 1328-8067            Impact factor:   1.524


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  2 in total

1.  PharmGKB summary: very important pharmacogene information for CACNA1S.

Authors:  Katrin Sangkuhl; Robert T Dirksen; Maria L Alvarellos; Russ B Altman; Teri E Klein
Journal:  Pharmacogenet Genomics       Date:  2020-02       Impact factor: 2.000

2.  The role of CACNA1S in predisposition to malignant hyperthermia.

Authors:  Danielle Carpenter; Christopher Ringrose; Vincenzo Leo; Andrew Morris; Rachel L Robinson; P Jane Halsall; Philip M Hopkins; Marie-Anne Shaw
Journal:  BMC Med Genet       Date:  2009-10-13       Impact factor: 2.103
  2 in total

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