Works by Fan, Xiaoge
Results: 2
HPDL mutations identified by exome sequencing are associated with infant neurodevelopmental disorders.
- Published in:
- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 10, p. 1, doi. 10.1002/mgg3.2025
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- Publication type:
- Article
Mild encephalitis/encephalopathy with a reversible splenial lesion associated with mumps infection: A case report.
- Published in:
- Pakistan Journal of Pharmaceutical Sciences, 2021, v. 34, n. 5, p. 1809, doi. 10.36721/PJPS.2021.34.5.REG.1809-1812.1
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- Publication type:
- Article