The human inward rectifying K+ channel Kir 2.2 (KXN12) gene: Gene structure, assignment to chromosome 17p11.1, and Identification of a simple tandem repeat polymorphism

Genomics

Volumn 39, Issue 1, 1997, Pages 113-116

  Hugnot, J P ^a   Pedeutour, F ^a   Le Calvez, C ^a   Grosgeorge, J ^a   Passage, E ^b   Fontes, M ^b   Lazdunski, M ^a  

^a CNRS   (France)

^b TIMONE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

POTASSIUM CHANNEL;

ARTICLE; CHROMOSOME 17P; DNA POLYMORPHISM; GENE DELETION; GENE ISOLATION; GENE LOCUS; GENE SEQUENCE; GENE STRUCTURE; HUMAN; PRIORITY JOURNAL; SMITH MAGENIS SYNDROME; TANDEM REPEAT;

EID: 0031033619     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.4450     Document Type: Article

References (25)

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