Frontiers Intrafamilial variability in SLC6A1-related neurodevelopmental disorders

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Last updated 22 dezembro 2024
Frontiers  Intrafamilial variability in SLC6A1-related neurodevelopmental  disorders
Frontiers  Intrafamilial variability in SLC6A1-related neurodevelopmental  disorders
Frontiers A defined method for differentiating human iPSCs into midbrain dopaminergic progenitors that safely restore motor deficits in Parkinson's disease
Frontiers  Intrafamilial variability in SLC6A1-related neurodevelopmental  disorders
Frontiers in Neuroscience
Frontiers  Intrafamilial variability in SLC6A1-related neurodevelopmental  disorders
Frontiers Phenotypic Trade-Offs: Deciphering the Impact of Neurodiversity on Drug Development in Fragile X Syndrome
Frontiers  Intrafamilial variability in SLC6A1-related neurodevelopmental  disorders
epilepsy type - List of Frontiers' open access articles
Frontiers  Intrafamilial variability in SLC6A1-related neurodevelopmental  disorders
PDF) The phenotypic presentation of adult individuals with SLC6A1-related neurodevelopmental disorders
Frontiers  Intrafamilial variability in SLC6A1-related neurodevelopmental  disorders
Spontaneous activity patterns in organotypic slice cultures of rat
Frontiers  Intrafamilial variability in SLC6A1-related neurodevelopmental  disorders
Frontiers Intrafamilial variability in SLC6A1-related neurodevelopmental disorders
Frontiers  Intrafamilial variability in SLC6A1-related neurodevelopmental  disorders
Katrine Johannesen — University of Southern Denmark
Frontiers  Intrafamilial variability in SLC6A1-related neurodevelopmental  disorders
Frontiers in Neuroscience
Frontiers  Intrafamilial variability in SLC6A1-related neurodevelopmental  disorders
Frontiers A draft conceptual model of SLC6A1 neurodevelopmental disorder
Frontiers  Intrafamilial variability in SLC6A1-related neurodevelopmental  disorders
PDF) Corrigendum: Intrafamilial variability in SLC6A1-related neurodevelopmental disorders
Frontiers  Intrafamilial variability in SLC6A1-related neurodevelopmental  disorders
PDF) A draft conceptual model of SLC6A1 neurodevelopmental disorder
Frontiers  Intrafamilial variability in SLC6A1-related neurodevelopmental  disorders
Frontiers A defined method for differentiating human iPSCs into midbrain dopaminergic progenitors that safely restore motor deficits in Parkinson's disease

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