Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3

Human Genetics

Volumn 106, Issue 6, 2000, Pages 614-619

  Postma, Alex V ^a,b   Bezzina, Connie R ^a,b   De Vries, Jeltje F ^b   Wilde, Arthur A M ^a   Moorman, Antoon F M ^a   Mannens, Marcel M A M ^b  

^a Laboratory for Physiology   (Netherlands)

^b ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ION CHANNEL; POTASSIUM; POTASSIUM CHANNEL;

ARTICLE; BRUGADA SYNDROME; CHROMOSOMAL LOCALIZATION; CHROMOSOME 1P; CHROMOSOME 7Q; EXON; GENE AMPLIFICATION; GENE MUTATION; GENE SEQUENCE; GENE STRUCTURE; HEART MUSCLE POTENTIAL; HUMAN; HUMAN CELL; INTRON; LONG QT SYNDROME; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

EID: 0033946873     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390000308     Document Type: Article

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