在患有脑部异常和发育迟缓的患者中,FBXO28的3' UTR删除
Xin Bi1, Maureen S Mulhern1,2, Erica Spiegel3
1Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA.
Genes
|September 28, 2023
概括
罕见的染色体1q42删除会导致发育迟缓和智力障碍. 这项研究确定了1q42.11中的特定63 kb删除,将FBXO28基因与1q41q42微删除综合征联系起来.
科学领域:
- 遗传学 是一个遗传学.
- 发展生物学 发展生物学
- 临床遗传学 临床遗传学
背景情况:
- 在1q42区域的宪法删除是不常见的遗传改变.
- 这些缺失与可变的表型谱有关,包括发育迟缓,智力障碍,发作和异形特征.
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