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138 results on '"Wu, Xiru"'

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9. Large De Novo Microdeletion in Epilepsy with Intellectual and Developmental Disabilities, with a Systems Biology Analysis

24. Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort

28. Nuclear Factor-κB Pathway Mediates the Molecular Pathogenesis of LMNA-Related Muscular Dystrophies

29. Clinical spectrum and genetic variations of LMNA-related muscular dystrophies in a large cohort of Chinese patients

39. Congenital muscular dystrophies in China

41. ATP1A3 mosaicism in families with alternating hemiplegia of childhood

49. Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy

50. Mosaicism and incomplete penetrance of PCDH19 mutations

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