Mutation is a Low-Incidence Genetic Cause in Atypical Rett Syndrome
Due to the genetic and clinical heterogeneity of Rett syndrome, patients with nonclassic phenotypes are classified as an atypical Rett syndrome, that is, preserved speech variant, early seizure variant, and congenital variant. Respectively, MECP2 , CDKL5 , and FOXG1 have been found to be the causati...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
SAGE Publishing
2015-03-01
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| Series: | Child Neurology Open |
| Online Access: | https://doi.org/10.1177/2329048X14568151 |