Bi-allelic truncating mutations in VWA1 cause neuromyopathy
by Deschauer, Marcus (Author)
, Hengel, Holger (Author)
, Rupprich, Katrin (Author)
, Kreiß, Martina (Author)
, Schlotter-Weigel, Beate (Author)
, Grimmel, Mona (Author)
, Admard, Jakob (Author)
, Schneider, Ilka (Author)
, Alhaddad, Bader (Author)
, Gazou, Anastasia (Author)
, Sturm, Marc (Author)
, Vorgerd, Matthias (Author)
, Balousha, Ghassan (Author)
, Balousha, Osama (Author)
, Falna, Mohammed (Author)
, Kirschke, Jan S. (Author)
, Kornblum, Cornelia (Author)
, Jordan, Berit (Author)
, Kraya, Torsten (Author)
, Strom, Tim M. (Author)
, Weis, Joachim (Author)
, Schöls, Ludger (Author)
, Schara, Ulrike (Author)
, Zierz, Stephan (Author)
, Riess, Olaf (Author)
, Meitinger, Thomas (Author)
, Haack, Tobias B. (Author)
,
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