Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleA Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmental Glomerulosclerosis with Alport Syndrome-like Phenotype.AuthorsYuji Oe; Eikan Mishima; Takayasu Mori; Koji Okamoto; Yohei Honkura; Tasuku Nagasawa; Mai Yoshida; Hiroshi Sato; Jun Suzuki; Ryoukichi Ikeda; Eisei Sohara; Shinichi Uchida; Yukio Katori; Mariko MiyazakiPublicationInternal Medicine, 2021, Vol 60, Issue 18, p2991ISSN0918-2918Publication typeArticleDOI10.2169/internalmedicine.6987-20