The molecular biology of FMRP: new insights into fragile X syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Neuroscience
Link
http://www.nature.com/articles/s41583-021-00432-0.pdf
Reference113 articles.
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3. Pieretti, M. et al. Absence of expression of the FMR-1 gene in fragile X syndrome. Cell 66, 817–822 (1991).
4. Verkerk, A. J. et al. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 65, 905–914 (1991).
5. Schaefer, G. B. & Mendelsohn, N. J. Genetics evaluation for the etiologic diagnosis of autism spectrum disorders. Genet. Med. 10, 4–12 (2008).
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