スポンサーリンク
Department Of Endocrinology And Metabolism Okinaka Memorial Institute For Medical Research And Toran | 論文
- Novel mutations of the FANCG gene causing alternative splicing in Japanese Fanconi anemia
- A Japanese Patient with Lipoprotein Lipase Deficiency Homozygous for the Gly188Glu Mutation Prevalent Worldwide
- Molecular characterization of Egyptian patients with glycogen storage disease type IIIa
- Mutational and haplotype analysis of AGL in patients with glycogen storage disease type III
- A Japanese Patient With Cardiomyopathy Caused by a Novel Mutation R285X in the AGL Gene
- Novel AGL mutation in a Turkish patient with glycogen storage disease type IIIa
- Molecular features of 23 patients with glycogen storage disease type III in Turkey : a novel mutation p.R1147G associated with isolated glucosidase deficiency, along with 9 AGL mutations
- Castleman's Disease Accompanied by Hypolipidemic Cerebral Hemorrhage and Nephrosclerosis