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2020
Doering, Jan Henje, Saffari, Afshin, Bast, Thomas, Brockmann, Knut 
ORCID: 0000-0001-6823-9091, Ehrhardt, Laura, Fazeli, Walid ORCID: 0000-0002-9425-5535, Janzarik, Wibke G., Kluger, Gerhard, Muhle, Hiltrud, Moller, Rikke S., Platzer, Konrad, Santos, Joana Larupa, Bache, Iben ORCID: 0000-0001-7562-8546, Bertsche, Astrid, Bonfert, Michaela, Borggraefe, Ingo, Broser, Philip J., Datta, Alexandre N., Hammer, Trine Bjorg, Hartmann, Hans, Hasse-Wittmer, Anette, Henneke, Marco, Kuehne, Hermann, Lemke, Johannes R., Maier, Oliver, Matzker, Eva, Merkenschlager, Andreas, Opp, Joachim, Patzer, Steffi, Rostasy, Kevin, Stark, Birgit, Strzelczyk, Adam, von Stuelpnagel, Celina, Weber, Yvonne, Wolff, Markus, Zirn, Birgit, Hoffmann, Georg Friedrich, Koelker, Stefan and Syrbe, Steffen
(2020).
The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood.
Biomedicines, 8 (11).
BASEL:
MDPI.
ISSN 2227-9059
2010
Boztug, Kaan ORCID: 0000-0001-8387-9185, Ding, Xiao-Qi, Hartmann, Hans, Ziesenitz, Lena, Schaeffer, Alejandro A., Diestelhorst, Jana, Pfeifer, Dietmar, Appaswamy, Giridharan, Kehbel, Sonja, Simon, Thorsten, Al Jefri, Abdullah, Lanfermann, Heinrich and Klein, Christoph
(2010).
HAX1 Mutations Causing Severe Congenital Neuropenia and Neurological Disease Lead to Cerebral Microstructural Abnormalities Documented by Quantitative MRI.
Am. J. Med. Genet. A, 152A (12).
S. 3157 - 3164.
HOBOKEN:
WILEY.
ISSN 1552-4833