Fragile X syndrome - insight into what we know and prospects

Fragile X syndrome - insight into what we know and prospects

Fragile X syndrome is a dominantly inherited genetic disease and is a consequence of the FMR1 gene mutation located on the X chromosome. The number of patients affected by this disease with full mutation is estimated at 1 in 4000 men and 1 in 8000 women, however, the number of carriers with premuta...

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Bibliographic Details
Main Authors: Adam Strzoda, Magdalena Kamińska, Anna Strzoda, Agata Strzoda, Wojciech Sowiński, Michał Zdybel, Agata Juda, Kornelia Rojek
Format: Article
Language:English
Published: Kazimierz Wielki University 2023-04-01
Series:Journal of Education, Health and Sport
Subjects:
Fragile X syndrome
autism
neurodevelopmental disorders
FMRP
FMR1
Online Access:https://apcz.umk.pl/JEHS/article/view/43229

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