1. Butler, Merlin G. 2023. Prader-Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review. In International journal of molecular sciences, 24, . doi:10.3390/ijms24054271. https://pubmed.ncbi.nlm.nih.gov/36901699/
2. Cox, Devin M, Butler, Merlin G. 2015. The 15q11.2 BP1-BP2 microdeletion syndrome: a review. In International journal of molecular sciences, 16, 4068-82. doi:10.3390/ijms16024068. https://pubmed.ncbi.nlm.nih.gov/25689425/
3. Jiang, Yuwu, Zhang, Yuehua, Zhang, Pingping, Chan, Piu, Wu, Xiru. 2012. NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy. In Human genetics, 131, 1217-24. doi:10.1007/s00439-012-1149-3. https://pubmed.ncbi.nlm.nih.gov/22367439/
4. Xie, Han, Zhang, Yuehua, Zhang, Pingping, Netoff, Theoden, Jiang, Yuwu. 2014. Functional study of NIPA2 mutations identified from the patients with childhood absence epilepsy. In PloS one, 9, e109749. doi:10.1371/journal.pone.0109749. https://pubmed.ncbi.nlm.nih.gov/25347071/
5. Butler, M G. 2017. Clinical and genetic aspects of the 15q11.2 BP1-BP2 microdeletion disorder. In Journal of intellectual disability research : JIDR, 61, 568-579. doi:10.1111/jir.12382. https://pubmed.ncbi.nlm.nih.gov/28387067/
6. Meossi, C, Carrer, A, Ciaccio, C, D'Arrigo, S, Milani, D. 2023. Clinical features and magnesium levels: Novel insights in 15q11.2 BP1-BP2 copy number variants. In Journal of intellectual disability research : JIDR, 67, 679-689. doi:10.1111/jir.13038. https://pubmed.ncbi.nlm.nih.gov/37129092/
7. Rafi, Syed K, Butler, Merlin G. 2020. The 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental Phenotypes. In International journal of molecular sciences, 21, . doi:10.3390/ijms21093296. https://pubmed.ncbi.nlm.nih.gov/32384786/
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