Dongyan Wu

Compound heterozygosity for novel variations of the NHLRC1 Gene in a family with Lafora disease

Yuncan Chen, Xinghua Tang, Xinjuan Li, 2022, Clinical Neurology and Neurosurgery.

Thyroid function in children with Prader-Willi syndrome in Southern China: a single-center retrospective case series

Wen Zhang, C. Zeng, Li Liu, 2022, BMC Pediatrics.

[Clinical features and StAR gene mutations in children with congenital lipoid adrenal hyperplasia].

T. Xie, Li Liu, Dongyan Wu, 2015, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

Clinical presentation and mutational spectrum in a series of 166 patients with classical 21-hydroxylase deficiency from South China.

Zhichun Feng, Li Liu, Yan-na Cai, 2018, Clinica chimica acta; international journal of clinical chemistry.

RBM20 is a candidate gene for hypertrophic cardiomyopathy.

Ting Yu, Q. Duan, Daowen Wang, 2021, The Canadian journal of cardiology.

Single-Point Mutation Near Active Center Increases Substrate Affinity of Alginate Lyase AlgL-CD

Xinqi Xu, Juan Lin, Dongyan Wu, 2021, Applied Biochemistry and Biotechnology.

First case report of medium-chain acyl-coenzyme A dehydrogenase deficiency in China

Li Liu, Yan-na Cai, H. Sheng, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

Clinical characteristics and long-term outcomes of 12 children with vitamin D-dependent rickets type 1A: A retrospective study

Wen Zhang, Yunting Lin, C. Zeng, 2022, Frontiers in Pediatrics.