Fragile X Syndrome : from diagnosis to treatment /
"Fragile X syndrome is an inherited disease caused by an excessive length of the FMR protein due to mutations in the FMR1 gene located on the X chromosome. It is commonly described as one of the most common genetic diseases with autism-like behaviors and related developmental disabilities. Besi...
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| Other Authors: | |
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| Format: | Electronic eBook |
| Language: | English |
| Published: |
New York :
Nova Science Publishers, Inc.,
[2022]
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| Series: | Genetics. Research and issues
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| Subjects: | |
| Online Access: | CONNECT |
