Bi-Allelic Truncating Mutations In Vwa1 Cause NeuromyopathyMarcus Deschauer,Holger Hengel,Katrin Rupprich,Martina Kreiß,Beate Schlotter-Weigel,Mona Grimmel,Jakob Admard,Ilka Schneider,Bader Alhaddad,Anastasia Gazou,Marc Sturm,Matthias Vorgerd,Ghassan Balousha,Osama Balousha, Mohammed Falna,Jan S Kirschke,Cornelia Kornblum,Berit Jordan,Torsten Kraya,Tim M Strom,Joachim Weis,Ludger Schöls,Ulrike Schara,Stephan Zierz,Olaf Riess,Thomas Meitinger,Tobias B HaackBRAIN（2021）引用 14|浏览31暂无评分关键词VWA1, mutations, neuromyopathy, exome sequencingAI 理解论文溯源树样例生成溯源树，研究论文发展脉络Chat Paper正在生成论文摘要
