6 results on '"Liu, Yedan"'
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2. Novel variants in TBC1D24 associated with epilepsy and deafness: Report of two cases
3. Levodopa is effective in the treatment of three Chinese Tyrosine hydroxylase (TH) deficiency children
4. The biochemical characterization of a missense mutation m.8914C>T in ATP6 gene associated with mitochondrial encephalomyopathy
5. Gene analysis: A rare gene disease of intellectual deficiency‐Cohen syndrome
6. A case of Pitt‐hopkins Syndrome with de novo mutation in TCF4: Clinical features and treatment for epilepsy
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