Zengge Wang

Carrier screening for spinal muscular atrophy with a simple test based on melting analysis

Zhongmin Xia, Yulin Zhou, Dongmei Fu et al. · Journal of Human Genetics · 2019 · 31 citations

Medicine, Diagnosis, Biostatistics +4

A gain-of-function TPC2 variant R210C increases affinity to PI(3,5)P2 and causes lysosome acidification and hypopigmentation

Qiaochu Wang, Zengge Wang, Yizhen Wang et al. · Nature Communications · 2023 · 28 citations · Full text

Clinical phenotype, in silico and biomedical analyses, and intervention for an East Asian population-specific c.370G>A (p.G124S) COQ4 mutation in a Chinese family with CoQ10 deficiency-associated Leigh syndrome

Mei Lu, Yulin Zhou, Zengge Wang et al. · Journal of Human Genetics · 2019 · 25 citations · Full text

Chinese Family, Mendelian Disorder, Coq4 Mutation +7

De novo truncating variant in NSD2gene leading to atypical Wolf-Hirschhorn syndrome phenotype

Yanrui Jiang, Huizhen Sun, Qingmin Lin et al. · BMC Medical Genetics · 2019 · 21 citations · Full text

The transcription factor Zeb1 controls homeostasis and function of type 1 conventional dendritic cells

Yan Wang, Quan Zhang, Tingting He et al. · Nature Communications · 2023 · 10 citations · Full text