Novel biallelic variants in IREB2 cause an early-onset neurodegenerative disorder in a Chinese pedigree.

Autor: Guo, Zhenglong1,2 (AUTHOR) zhenglongguo@zzu.edu.cn, Huo, Dawei3 (AUTHOR), Shao, Yingying4 (AUTHOR), Yang, Wenke1,2 (AUTHOR), Wang, Jinming1,2 (AUTHOR), Zhang, Yuwei1,2 (AUTHOR), Xiao, Hai1,2 (AUTHOR), Hao, Bingtao1,5,6 (AUTHOR) haobt123@zzu.edu.cn, Liao, Shixiu1,2 (AUTHOR) ychslshx@henu.edu.cn
Zdroj: Orphanet Journal of Rare Diseases. 11/25/2024, Vol. 19 Issue 1, p1-9. 9p.
Databáze: Academic Search Ultimate
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