New human sodium/glucose cotransporter gene (KST1): identification, characterization, and mutation analysis in ICCA (infantile convulsions and choreoathetosis) and BFIC (benign familial infantile convulsions) families
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
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3. Channelopathies: ion channel defects linked to heritable clinical disorders;Felix;J. Med. Genet.,2000
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5. cDNA sequence for rkST1, a novel member of the sodium ion-dependent glucose cotransporter family;Hitomi;Biochim. Biophys. Acta,1994
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