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is ?:annotates of
?:creator
?:journal
  • Neurol._sci
?:license
  • unk
?:publication_isRelatedTo_Disease
?:source
  • WHO
?:title
  • A de novo mutation in SMC1A gene identified in a Chinese infant with nonclassical Cornelia de Lange syndrome and drug-resistant epilepsy
?:type
?:who_covidence_id
  • #32648047
?:year
  • 2020

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