Journalartikel
Autorenliste: Michalakis, Stylianos; Shaltiel, Lior; Sothilingam, Vithiyanjali; Koch, Susanne; Schludi, Verena; Krause, Stefanie; Zeitz, Christina; Audo, Isabelle; Lancelot, Marie-Elise; Hamel, Christian; Meunier, Isabelle; Preising, Markus N.; Friedburg, Christoph; Lorenz, Birgit; Zabouri, Nawal; Haverkamp, Silke; Garrido, Marina Garcia; Tanimoto, Naoyuki; Seeliger, Mathias W.; Biel, Martin; Wahl-Schott, Christian A.
Jahr der Veröffentlichung: 2017
Seiten: 466-466
Zeitschrift: Human Molecular Genetics
Bandnummer: 26
Heftnummer: 2
ISSN: 0964-6906
eISSN: 1460-2083
Open Access Status: Green
DOI Link: https://doi.org/10.1093/hmg/ddw424
Verlag: Oxford University Press
Zitierstile
Harvard-Zitierstil: Michalakis, S., Shaltiel, L., Sothilingam, V., Koch, S., Schludi, V., Krause, S., et al. (2017) Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2 (vol 23, pg 1538, 2014), Human Molecular Genetics, 26(2), p. 466. https://doi.org/10.1093/hmg/ddw424
APA-Zitierstil: Michalakis, S., Shaltiel, L., Sothilingam, V., Koch, S., Schludi, V., Krause, S., Zeitz, C., Audo, I., Lancelot, M., Hamel, C., Meunier, I., Preising, M., Friedburg, C., Lorenz, B., Zabouri, N., Haverkamp, S., Garrido, M., Tanimoto, N., Seeliger, M., ...Wahl-Schott, C. (2017). Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2 (vol 23, pg 1538, 2014). Human Molecular Genetics. 26(2), 466. https://doi.org/10.1093/hmg/ddw424
