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
β¦ LIBER β¦
A Mouse Model of the Human Fragile X Syndrome I304N Mutation
β Scribed by Zang, Julie B.; Nosyreva, Elena D.; Spencer, Corinne M.; Volk, Lenora J.; Musunuru, Kiran; Zhong, Ru; Stone, Elizabeth F.; Yuva-Paylor, Lisa A.; Huber, Kimberly M.; Paylor, Richard; Darnell, Jennifer C.; Darnell, Robert B.; Cox, Gregory A.
- Book ID
- 120370878
- Publisher
- Public Library of Science
- Year
- 2009
- Tongue
- English
- Weight
- 955 KB
- Volume
- 5
- Category
- Article
- ISSN
- 1553-7390
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