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• W2485498977 endingPage "41" @default.
• W2485498977 startingPage "25" @default.
• W2485498977 abstract "Intellectual disability (ID) represents a heterogeneous disorder affecting the development, function, and/or structure of the central nervous system. ID affects about 2–3% of the general population, with a male excess estimated around 30%. Genetic defects on the X chromosome are supposed to have a major role in this gender bias. X-linked intellectual disability (XLID) can be grouped into two categories, syndromal and nonsyndromal, although some genes can be responsible for both forms. In the past 2 decades, important progress has been made in identifying new causative genes and understanding the disease mechanisms underlying over 100 XLID conditions. Most known genes involve one of the following functional groups: presynaptic vesicle cycling and transport, cytoskeletal dynamics, cell adhesion and transsynaptic signaling, and translational regulation. Expanding knowledge of XLID also allows researchers to design new therapeutic approaches." @default.
• W2485498977 created "2016-08-23" @default.
• W2485498977 creator A5039616601 @default.
• W2485498977 creator A5072815495 @default.
• W2485498977 date "2016-01-01" @default.
• W2485498977 modified "2023-09-30" @default.
• W2485498977 title "Genetics of X-Linked Intellectual Disability" @default.
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