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• W2599452621 abstract "HERC1 is a member of HERC protein family of ubiquitin ligases and is a negative regulator of the mTOR pathway. It is also a guanine nucleotide exchange factor for ARF and Rab family GTPases. Biallelic mutations in HERC1 were recently shown to cause a human phenotype with overgrowth and intellectual disability as main features. Herein we describe clinical features in another patient with homozygous novel mutation in HERC1. Moderate to severe intellectual disability, hypotonia, macrocephaly, tall stature, and facial features appear as main clinical features of the condition. Kyphoscoliosis and seizures frequently accompany and autistic features might be another feature as recent studies also implicate. HERC1 mutations should be considered in differential diagnosis of severe intellectual disability and behavioural problems, particularly in patients testing negative for fragile X and KANSL1 mutations." @default.
• W2599452621 created "2017-04-07" @default.
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• W2599452621 date "2017-05-01" @default.
• W2599452621 modified "2023-09-24" @default.
• W2599452621 title "HERC1 mutations in idiopathic intellectual disability" @default.
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• W2599452621 doi "https://doi.org/10.1016/j.ejmg.2017.03.007" @default.
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