Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Joanna Janina Lerner"'
Autor:
Mariagiovanna Malara, Anne-Kathrin Lutz, Berra Incearap, Helen Friedericke Bauer, Silvia Cursano, Katrin Volbracht, Joanna Janina Lerner, Rakshita Pandey, Jan Philipp Delling, Valentin Ioannidis, Andrea Pérez Arévalo, Jaime Eugenin von Bernhardi, Michael Schön, Jürgen Bockmann, Leda Dimou, Tobias M. Boeckers
Publikováno v:
Cellular and molecular life sciences 79(7), 371 (2022). doi:10.1007/s00018-022-04400-4
Mutations or deletions of the SHANK3 gene are causative for Phelan–McDermid syndrome (PMDS), a syndromic form of autism spectrum disorders (ASDs). We analyzed Shank3Δ11(−/−) mice and organoids from PMDS individuals to study effects on myelin.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41b56ee830d7ba63e564f78a8fbf9d41
