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pro vyhledávání: '"I I Joseph Foster"'
Autor:
Michelle Moffat, Juan I. Young, Katherina Walz, Paolo Curatolo, Kathrine Bjørgo, Lily Zhang, Devon Cohen, Korcan Demir, Francesco Brancati, Giuseppe Novelli, Oscar Diaz-Horta, Adriana Lo Castro, Paul M. Neilsen, Nienke E. Verbeek, David F. Callen, Mustafa Tekin, Clemer Abad, I I Joseph Foster, Cao Lei, Richard Fisher
Publikováno v:
Human Genetics, 134(2), 181. Springer Verlag
Mutations in ANKRD11 have recently been reported to cause KBG syndrome, an autosomal dominant condition characterized by intellectual disability (ID), behavioral problems, and macrodontia. To understand the pathogenic mechanism that relates ANKRD11 m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fd6450767e69cc7dca5f0bac4295ee4
http://hdl.handle.net/11697/122716
http://hdl.handle.net/11697/122716
