Subject
Genetics (clinical),Genetics,General Medicine
Reference28 articles.
1. Delineating the genotypic and phenotypic spectrum of HECW2-related neurodevelopmental disorders;Acharya;J. Med. Genet.,2021
2. De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia;Berko;J. Med. Genet.,2017
3. Clinical and genetic investigations of three Moroccan families with retinitis pigmentosa phenotypes;Bouzidi;Mol. Vis.,2021
4. Expression of the CDH1-associated form of the anaphase-promoting complex in postmitotic neurons;Gieffers;Proc. Natl. Acad. Sci. U. S. A,1999
5. Mutations in HECW2 are associated with intellectual disability and epilepsy;Halvardson;J. Med. Genet.,2016
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