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

Gene

Volumn 285, Issue 1-2, 2002, Pages 141-148

  Roll, Patrice ^a   Massacrier, Annick ^a   Pereira, Sandrine ^a   Robaglia Schlupp, Andrée ^a   Cau, Pierre ^a   Szepetowski, Pierre ^a  

^a INSERM   (France)

Author keywords

16p12 p11; KST1; Sodium glucose cotransporter

Indexed keywords

COMPLEMENTARY DNA; GLUCOSE TRANSPORTER; PROTEIN KST1; RNA; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BENIGN FAMILIAL INFANTILE CONVULSION; CHROMOSOME 16P; CONTROLLED STUDY; DNA POLYMORPHISM; EXON; GENE AMPLIFICATION; GENE EXPRESSION; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC CODE; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; GLUCOSE TRANSPORT; HUMAN; HUMAN GENOME; HUMAN TISSUE; INFANTILE CONVULSIONS AND CHOREOATHETOSIS SYNDROME; NUCLEOTIDE SEQUENCE; ORTHOLOGY; PRIORITY JOURNAL; PROTEIN DOMAIN; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA SPLICING; SODIUM TRANSPORT;

ORYCTOLAGUS CUNICULUS;

EID: 0037138392     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(02)00416-X     Document Type: Article

References (24)

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