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
PubMed
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.