Author

S T Wang

Institution: Qingdao University

Observed institution: Qingdao University

OpenAlex ID: A5011500473

[A case of neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination caused by a variant in NACC1 gene].

2024 · D R Sun, S T Wang, et al. · PubMed

Works count: 1

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