论文信息 - hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes - 字舞流文

hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes

D. Hannequin | A. Brice | D. Wallon | A. Camuzat | E. Kabashi | G. Nicolas | I. Ber | S. Lattante | M. Latouche | L. Jornéa | A. Septenville | Kawtar Bouya-Ahmed | Inge Van Bortel | Morwena Latouche | Ludmila Jornea