Associated Papers
A Heterozygous Variant of FGF13 Caused X-Linked Developmental and Epileptic Encephalopathy 90 in a Chinese Family.
Cheng H et al.
Cytogenetic and Genome Research, 2023
Monoamine neurotransmitters in early epileptic encephalopathies: New insights into pathophysiology and therapy.
Juliá-Palacios N et al.
Developmental Medicine and Child Neurology, 2022
Further evidence of affected females with a heterozygous variant in FGF13 causing X-linked developmental and epileptic encephalopathy 90.
Narayanan DL et al.
European Journal of Medical Genetics, 2022
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