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pro vyhledávání: '"Charles Austria"'
Autor:
Jason W. Adams, Annabelle Vinokur, Janaína S. de Souza, Charles Austria, Bruno S. Guerra, Roberto H. Herai, Karl J. Wahlin, Alysson R. Muotri
Publikováno v:
Cell Reports, Vol 43, Iss 3, Pp 113867- (2024)
Summary: Individuals with Williams syndrome (WS), a neurodevelopmental disorder caused by hemizygous loss of 26–28 genes at 7q11.23, characteristically portray a hypersocial phenotype. Copy-number variations and mutations in one of these genes, GTF
Externí odkaz:
https://doaj.org/article/77e344c08eb6407895cdd8d2439e33a3
