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Autor:
Roberta Pietrobono, Veronica Nobile, Maria Grazia Pomponi, Giovanni Neri, Laura Remondini, Elisabetta Tabolacci, Fiorella Gurrieri, Pietro Chiurazzi, Gaetana Pennacchio, Maurizio Genuardi
Publikováno v:
Eur J Hum Genet
Fragile X syndrome (FXS) is a very frequent cause of inherited intellectual disability (ID) and autism. Most FXS patients have an expansion over 200 repeats of (CGG)(n) sequence (“full mutation” (FM)) located in the 5′UTR of the FMR1 gene, resu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b2eb1d2f06e7181155dd1460ed5f31b
http://hdl.handle.net/10807/147818
http://hdl.handle.net/10807/147818
