A novel heterozygous ZBTB18 missense mutation in a family with non-syndromic intellectual disability
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Genetics (clinical),Genetics
Link
https://link.springer.com/content/pdf/10.1007/s10048-023-00727-7.pdf
Reference61 articles.
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2. Moeschler JB, Shevell M (2014) Comprehensive evaluation of the child with intellectual disability or global developmental delays. Pediatrics 134(3):e903–e918
3. Vissers LE, Gilissen C, Veltman JA (2016) Genetic studies in intellectual disability and related disorders. Nat Rev Genet 17(1):9–18
4. Vasudevan P, Suri M (2017) A clinical approach to developmental delay and intellectual disability. Clin Med 17(6):558–561
5. Feldkamp ML, Carey JC, Byrne JLB, Krikov S, Botto LD (2017) Etiology and clinical presentation of birth defects: population based study. BMJ 357:j2249
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