_id,doi,title
14543,10.1093/brain/awad380,Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders
12174,10.1093/brain/awac145,Phenotypic and genetic spectrum of ATP6V1A encephalopathy: A disorder of lysosomal homeostasis
12212,10.1186/s13195-022-01078-5,Nanoscale alterations in GABAB receptors and GIRK channel organization on the hippocampus of APP/PS1 mice