Newly discovered variants in unexplained neonatal encephalopathy

ConclusionOur study expands the mutation spectrum of genes associated with NE and introduces new evidence for molecular diagnosis in this newborn illness.

https://onlinelibrary.wiley.com/doi/10.1002/mgg3.2354?af=R

Source: Molecular Genetics & Genomic Medicine - January 18, 2024 Category: Genetics & Stem Cells Authors: Rong Zhang, Jingjing Xie, Xiao Yuan, Yan Yu, Yan Zhuang, Fan Zhang, Jianfei Hou, Yanqin Liu, Weiqing Huang, Min Zhang, Junshuai Li, Qiang Gong, Xiaoming Peng Tags: ORIGINAL ARTICLE Source Type: research