Aoyama Yoshiko | Okinaka Memorial Inst. For Medical Res. Tokyo Jpn

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概要

• 同名の論文著者
• Okinaka Memorial Inst. For Medical Res. Tokyo Jpnの論文著者

関連著者

• Aoyama Yoshiko

  Okinaka Memorial Inst. For Medical Res. Tokyo Jpn

• Aoyama Yoshiko

  Okinaka Memorial Institute For Medical Research

• Murase T

  Okinaka Memorial Institute For Medical Research

• EBARA Tetsu

  Okinaka Memorial Institute for Medical Research

• MURASE Toshio

  Okinaka Memorial Institute for Medical Research

• OKUBO Minoru

  Okinaka Memorial Institute for Medical Research

• Shin Yoon

  Molecular Genetics And Metabolism Laboratory

• Murase T

  Department Of Endocrinology And Metabolism Okinaka Memorial Institute For Medical Research And Toran

• Ozer Isil

  Department Of Pediatric Nutrition And Metabolism Istanbul Medical Faculty Istanbul University

• Demirkol Mubeccel

  Department Of Pediatric Nutrition And Metabolism Istanbul Medical Faculty Istanbul University

• ENDO Yoriko

  Okinaka Memorial Institute for Medical Research

• PODSKARBI Teodor

  Molecular Genetics and Metabolism Laboratory

• GOKCAY Gulden

  Department of Pediatric Nutrition and Metabolism, Istanbul Medical Faculty, Istanbul University

• Gokcay Gulden

  Department Of Pediatric Nutrition And Metabolism Istanbul Medical Faculty Istanbul University

• FATEEN Ekram

  Biochemical Genetics Department, National Research Centre

• HORINISHI Asako

  Okinaka Memorial Institute for Medical Research

• SHIN Yoon

  Department of Pediatrics, University of Muenchen

• Fateen Ekram

  Biochemical Genetics Department National Research Centre

• Horinishi Asako

  Okinaka Memorial Inst. For Medical Res. Tokyo Jpn

• DEMIRKOL Mubeccel

  Department of Pediatric Nutrition and Metabolism, Istanbul Medical Faculty, Istanbul University

• Shin Yoon

  Department Of Pediatrics And Institute Of Allergy Yonsei University College Of Medicine

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著作論文

• Molecular characterization of Egyptian patients with glycogen storage disease type IIIa
• Molecular features of 23 patients with glycogen storage disease type 3 in Turkey: a novel mutation p.R1147G associated with isolated glucosidase deficiency, along with 9 AGL mutations
• 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

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