Genetically determined encephalopathy
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Publisher
Elsevier
Reference42 articles.
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2. CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients;Archer;J Med Genet,2006
3. FOXG1 is responsible for the congenital variant of Rett syndrome;Ariani;Am J Hum Genet,2008
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4. Lower incidence of fracture after IV bisphosphonates in girls with Rett syndrome and severe bone fragility;PLOS ONE;2017-10-26
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