[1P] F. Disorders of the Nervous System 2

[1P-300] A low amyloidogenic E61K transthyretin mutation causes familial amyloid polyneuropathy: the mechanism of neurodegeneration

*Tatsufumi Murakami¹, Mineykuki Mizuguchi², Kazunori Sango³, Shigenobu Tone⁴, Yoshihide Sunada¹ (1. Kawasaki Medical School, 2. Toyama Medical and Pharmaceutical University, 3. Tokyo Metropolitan Institute of Medical Science, 4. Tokyo Denki University)

Keywords:

AMYLOID,DRG,NEUROPATHY,TRANSTHYRETIN

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PW: Neuro2022