Associated Papers
Neuropsychological Characterization of Autosomal Recessive Intellectual Developmental Disorder 59 Associated with IMPA1 (MRT59).
Pessoa ALS et al.
Brain Sciences, 2023
Inositol monophosphatase 1 (IMPA1) mutation in intellectual disability patients impairs neurogenesis but not gliogenesis.
Figueiredo T et al.
Molecular Psychiatry, 2021
Loss-of-function mutation in inositol monophosphatase 1 (IMPA1) results in abnormal synchrony in resting-state EEG.
Walker CP et al.
Orphanet Journal of Rare Diseases, 2019
A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability.
Figueiredo T et al.
Molecular Psychiatry, 2016
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