Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Pierre Cattenoz"'
Autor:
Valeria Specchia, Simona D’Attis, Antonietta Puricella, Pierre Cattenoz, Angela Giangrande, Maria Pia Bozzetti
Fragile-X Syndrome represents the most common form of hereditary mental retardation. The disorder originates with mutations in the Fmr1 gene coding for the FMRP protein, which, with its paralogs FXR1 and FXR2, constitute a well-conserved family of RN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4034::f650e663733bcdbceb03393af49a7378
https://hdl.handle.net/11587/441621
https://hdl.handle.net/11587/441621