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...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Kazimierz Wielki University
2023-04-01
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Series: | Journal of Education, Health and Sport |
Subjects: | |
Online Access: | https://apcz.umk.pl/JEHS/article/view/43229 |