R. Frank Kooy,Rudi D’Hooge,Edwin Reyniers,Cathy E. Bakker,Guy Nagels,Kristel De Boulle,Katrien Storm,Gilbert Clincke,Peter P. De Deyn,Ben A. Oostra,Patrick J. Willems
出处
期刊:American journal of medical genetics [Wiley] 日期:1996-08-09卷期号:64 (2): 241-245被引量:181
Transgenic fragile X knockout mice have been constructed to provide an animal model to study the physiologic function of the fragile X gene (FMR1) and to gain more insight into the clinical phenotype caused by the absence of the fragile X protein. Initial experiments suggested that the knockout mice show macroorchidism and cognitive and behavioral deficits, abnormalities comparable to those of human fragile X patients. In the present study, we have extended our experiments, and conclude that the Fmr1 knockout mouse is a reliable transgenic model to study the fragile X syndrome.