A heterozygous female with Fabry disease due to a novel alpha-galactosidase A mutation exhibits a unique synaptopodin distribution in vacuolated podocytes
A heterozygous female with Fabry disease due to a novel alpha-galactosidase A mutation exhibits a unique synaptopodin distribution in vacuolated podocytes
复制标题
由于新型 α-半乳糖苷酶 A 突变而患有法布里病的杂合女性在空泡足细胞中表现出独特的突触蛋白分布
作者：
N.Takahashi;S.Yokoi;K.Kasuno;A.Kogami;T.Tsukimura;T.Togawa;S.Saito;K.Ohno;M.Hara;H.Kurosawa;Y.Hirayama;T.Kurose;Y.Yokoyama;D.Mikami;H.Kimura;H.Naiki;H.Sakuraba;M.Iwano
