Hua Wang
5PUBLICATIONS
8CO-AUTHORS
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Publications (5)
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|Nov 14, 2023
De novo variants in KCNJ3 are associated with early-onset epilepsy.Juan Li, Shiyue Mei, Xiao Mao
|Jul 20, 2022
A de novo inframe deletion variant in CAPZA2 tentacle domain with global developmental delay and secondary microcephaly.Shanyu Pi, Xiao Mao, Hongyu Long
|May 31, 2022
Compound heterozygous variants in MAN2B2 identified in a Chinese child with congenital disorders of glycosylation.Qi Tian, Li Shu, Chuqiang Shu
|Aug 22, 2020
De novo missense variants in LMBRD2 are associated with developmental and motor delays, brain structure abnormalities and dysmorphic features.Alka Malhotra, Alban Ziegler, Li Shu
|Aug 01, 2019
Molecular investigation in Chinese patients with primary carnitine deficiency.Yanghui Zhang, Haoxian Li, Jing Liu
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