R306X Mutation in the Gene Causes an Atypical Rett Syndrome in a Moroccan Patient: A Case Report
Rett syndrome (RTT) is a rare X-linked syndrome that predominantly affects girls. It is characterized by a severe and progressive neurodevelopmental disorder with neurological regression and autism spectrum features. The Rett syndrome is associated with a broad phenotypic spectrum. It ranges from a...
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| Main Authors: | , , , , |
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| Format: | Book |
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SAGE Publishing,
2022-09-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |