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Heterogeneity of FHF1 related phenotype: Novel case with early onset severe attacks of apnea, partial mitochondrial respiratory chain complex II deficiency, neonatal onset seizures without neurodegeneration

Neurodegenerative DiseasesMendelian DisorderNovel CaseDisease MechanismGenetic DisorderMedicineGeneticsGenetic EpidemiologyFhf1 Related PhenotypeDegenerative DiseaseNeurologyNeuropathologyNeonatal Onset SeizuresNeurogenetics