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1 Ergebnisse
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Bi-allelic truncating mutations in VWA1 cause neuromyopathy:
Deschauer, Marcus
;
Hengel, Holger
;
Rupprich, Katrin
...
Brain. 144 (2021) 2 - p. 574-583 , 2021
Link:
https://doi.org/10.1093/brain/awaa418
RT Journal T1
Bi-allelic truncating mutations in VWA1 cause neuromyopathy
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_brain_awaa418&Exemplar=1&LAN=DE A1 Deschauer, Marcus A1 Hengel, Holger A1 Rupprich, Katrin A1 Kreiß, Martina A1 Schlotter-Weigel, Beate A1 Grimmel, Mona A1 Admard, Jakob A1 Schneider, Ilka A1 Alhaddad, Bader A1 Gazou, Anastasia A1 Sturm, Marc A1 Vorgerd, Matthias A1 Balousha, Ghassan A1 Balousha, Osama A1 Falna, Mohammed A1 Kirschke, Jan S A1 Kornblum, Cornelia A1 Jordan, Berit A1 Kraya, Torsten A1 Strom, Tim M A1 Weis, Joachim A1 Schöls, Ludger A1 Schara, Ulrike A1 Zierz, Stephan A1 Riess, Olaf A1 Meitinger, Thomas A1 Haack, Tobias B PB Oxford University Press (OUP) YR 2021 SN 0006-8950 SN 1460-2156 JF Brain VO 144 IS 2 SP 574 OP 583 LK http://dx.doi.org/https://doi.org/10.1093/brain/awaa418 DO https://doi.org/10.1093/brain/awaa418 SF ELIB - SuUB Bremen
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