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pro vyhledávání: '"Suchy, Christine"'
Autor:
Straub, Jonas, Gregor, Anne, Sauerer, Tatjana, Fliedner, Anna, Distel, Laila, Suchy, Christine, Ekici, Arif B., Ferrazzi, Fulvia, Zweier, Christiane
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Publons
Scientific Reports
Publons
Scientific Reports
Neurodevelopmental disorders (NDDs) are clinically and genetically extremely heterogeneous with shared phenotypes often associated with genes from the same networks. Mutations in TCF4, MEF2C, UBE3A, ZEB2 or ATRX cause phenotypically overlapping, synd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8f9ba1042518a6b36997a39dba648f31
http://link.springer.com/article/10.1038/s41598-020-58182-5
http://link.springer.com/article/10.1038/s41598-020-58182-5
