The functional consequences of SCN2A mutations determine the phenotype
Begemann A, Acuna M, Zweier M, Sticht H, Steindl K, Besnard M, Hackenberg A, Abela L, Plecko B, Yamakawa K, Inoue Y, Baumer A, Joset P, Asadollahi R, Zeilhofer H, Rauch A (2019)
Publication Type: Conference contribution
Publication year: 2019
Journal
Publisher: NATURE PUBLISHING GROUP
City/Town: LONDON
Pages Range: 240-240
Conference Proceedings Title: EUROPEAN JOURNAL OF HUMAN GENETICS
Event location: Milan
Authors with CRIS profile
Involved external institutions
University of Zurich / Universität Zürich (UZH)
Switzerland (CH)
Riken Institute of Physical and Chemical Research / 理研
Japan (JP)
Universitäts-Kinderspital Zürich
Switzerland (CH)
Shizuoka Institute of Epilepsy and Neurological Disorders
Japan (JP)
Switzerland (CH)
Riken Institute of Physical and Chemical Research / 理研
Japan (JP)
Universitäts-Kinderspital Zürich
Switzerland (CH)
Shizuoka Institute of Epilepsy and Neurological Disorders
Japan (JP)
How to cite
APA:
Begemann, A., Acuna, M., Zweier, M., Sticht, H., Steindl, K., Besnard, M.,... Rauch, A. (2019). The functional consequences of SCN2A mutations determine the phenotype. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 240-240). Milan, IT: LONDON: NATURE PUBLISHING GROUP.
MLA:
Begemann, A., et al. "The functional consequences of SCN2A mutations determine the phenotype." Proceedings of the 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan LONDON: NATURE PUBLISHING GROUP, 2019. 240-240.
BibTeX: Download