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1. GM1 gangliosidosis type II: Results of a 10-year prospective study

5. Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

6. Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

10. Association of brain-derived neurotrophic factor (BDNF) haploinsufficiency with lower adaptive behaviour and reduced cognitive functioning in WAGR/11p13 deletion syndrome

11. Contributors

16. Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

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