Screening for fmr1 expanded alleles in patients with autism spectrum disorders in Manaus, Northern Brazil
Fragile X Syndrome (FXS) is a neurodevelopmental disorder caused by dynamic mutations of a CGG repetition segment in an X chromosome’s single gene. It is considered the leading hereditary cause of both Autism Spectrum Disorders and Intellectual Disability. Some authors suggest that all individuals d...
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| Outros Autores: | , |
| Formato: | article |
| Idioma: | eng |
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2020
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| Texto completo: | https://doi.org/10.1590/0001-3765201920180882 |
| País: | Brasil |
| Oai: | oai:repositorio:1/14886 |