1. von Elsner, Leonie, Chai, Guoliang, Schneeberger, Pauline E, Gleeson, Joseph G, Kutsche, Kerstin. . Biallelic FRA10AC1 variants cause a neurodevelopmental disorder with growth retardation. In Brain : a journal of neurology, 145, 1551-1563. doi:10.1093/brain/awab403. https://pubmed.ncbi.nlm.nih.gov/34694367/
2. Alsaleh, Norah, Alhashem, Amal, Tabarki, Brahim, Alkuraya, Fowzan S, Almontashiri, Naif A M. 2022. A Biallelic Variant in FRA10AC1 Is Associated With Neurodevelopmental Disorder and Growth Retardation. In Neurology. Genetics, 8, e200010. doi:10.1212/NXG.0000000000200010. https://pubmed.ncbi.nlm.nih.gov/35821753/
3. Annear, Dale J, Kooy, R Frank. . Unravelling the link between neurodevelopmental disorders and short tandem CGG-repeat expansions. In Emerging topics in life sciences, 7, 265-275. doi:10.1042/ETLS20230021. https://pubmed.ncbi.nlm.nih.gov/37768318/
4. Banka, Siddharth, Shalev, Stavit, Park, Soo-Mi, Zeef, Leo A H, O'Keefe, Raymond T. . Bi-allelic FRA10AC1 variants in a multisystem human syndrome. In Brain : a journal of neurology, 145, e86-e89. doi:10.1093/brain/awac262. https://pubmed.ncbi.nlm.nih.gov/35871492/
5. Li, Qingqin S, Parrado, Antonio R, Samtani, Mahesh N, Narayan, Vaibhav A. 2015. Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. In PloS one, 10, e0134000. doi:10.1371/journal.pone.0134000. https://pubmed.ncbi.nlm.nih.gov/26252872/
智鼠故事 
