Localization of the human caveolin-3 gene to the D3S18/D3S4163/D3S4539 locus (3p25), in close proximity to the human oxytocin receptor geneIdentification of the caveolin-3 gene as a candidate for deletion in 3p-syndrome

FEBS Letters

Volumn 452, Issue 3, 1999, Pages 177-180

  Sotgia, Federica ^a,b   Minetti, Carlo ^b   Lisanti, Michael P ^a  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF GENOA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CAVEOLIN; MICROSATELLITE DNA; OXYTOCIN RECEPTOR;

ARTICLE; CHROMOSOME DELETION; CONTROLLED STUDY; GENE DELETION; GENE LOCATION; HEART DILATATION; HUMAN; HUMAN CELL; PATHOGENESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SKELETAL MUSCLE; VON HIPPEL LINDAU DISEASE;

BASE SEQUENCE; CAVEOLIN 3; CAVEOLINS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 3; DNA PRIMERS; EXONS; GENE DELETION; GENETIC MARKERS; HEART SEPTAL DEFECTS; HIPPEL-LINDAU DISEASE; HUMANS; MEMBRANE PROTEINS; MICROSATELLITE REPEATS; MUSCLE PROTEINS; MUSCLE, SKELETAL; MYOCARDIUM; RECEPTORS, OXYTOCIN; SYNDROME;

STAPHYLOCOCCUS PHAGE 3A;

EID: 0032965439     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-5793(99)00658-4     Document Type: Article

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