Familial amyloid polyneuropathy involving a homozygous Val30Met mutation in the amyloidogenic transthyretin gene presenting with superficial siderosis: a case report
古典型脳表ヘモジデリン沈着症を呈したVal30Metホモ接合体家族性アミロイドポリニューロパチーの1例

Yuta Maetani, Dai Agari, Eiichi Nomura, Mitsuharu Ueda, Yukio Ando, Takemori Yamawaki
2016 Rinsho Shinkeigaku  
doi:10.5692/clinicalneurol.cn-000869 pmid:27212678 fatcat:auk3lgrjwrdg7h4bhgtuhifmiu