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pro vyhledávání: '"Andrea Wiegers"'
Autor:
Catarina Martins-Costa, Vincent A. Pham, Andrea Wiegers, Jaydeep Sidhaye, Balint Doleschall, Maria Novatchkova, Thomas Lendl, Marielle Piber, Angela Peer, Paul Möseneder, Marlene Stuempflen, Siu Yu A. Chow, Rainer Seidl, Daniela Prayer, Romana Höftberger, Gregor Kasprian, Yoshiho Ikeuchi, Nina S. Corsini, Jürgen A. Knoblich
Mutations inARID1B, a member of the mSWI/SNF complex, cause severe neurodevelopmental phenotypes with elusive mechanisms in humans. The most common structural abnormality in the brain of ARID1B patients is agenesis of the corpus callosum (ACC). This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c42cd9e8a8065f9d53c01d8257cbc6da
https://doi.org/10.1101/2023.05.04.539362
https://doi.org/10.1101/2023.05.04.539362
