[Pj-072] Metabolic disorders (Clinical genetics2)

[Pj-072-2] A family with leukoencephalopathy carrying COX10 mutation and deletion of PMP22: clinical analysis

^○Yasuko Kuroha^1,2, Takanobu Ishiguro^2,4, Arika Hasegawa¹, Takashi Tani¹, Tetsuya Takahashi¹, Nae Matsubara¹, Mari Tada³, Izumi Kawachi⁴, Akiyoshi Kakita³, Osamu Onodera⁴, Takeshi Ikeuchi², Ryoko Koike¹ (1.Department of Neurology, Nishi-Niigata chuo National Hospital, 2.Department of Neurology, Moleular Genetics, Brain Research Institute, Niigata University, 3.Department of Pathology, Brain Research Institute, Niigata University, 4.Department of Neurology, Brain Research Institute, Niigata University)