Siblings of acyl CoA oxidase deficiency caused by a novel ACOX1 gene mutation

Takashi Enokizono

Presentation information

Oral Presentation

Neurodegenerative disease

[O28] Neurodegenerative disease

Fri. Jun 1, 2018 2:40 PM - 3:30 PM Room 9 (1F 104)

Chair:Kazuhiro Haginoya(Department of Pediatric Neurology, Miyagi Children's Hospital), HITOSHI OSAKA(Dept. of Pediatrics, Jichi Medical School, Shimotsuke, Japan)

[O-157] Siblings of acyl CoA oxidase deficiency caused by a novel ACOX1 gene mutation

Takashi Enokizono¹, Nobuyuki Shimozawa², Atsushi Morita¹, Shiena Watanabe¹, Mai Tanaka¹, Tatsuyuki Ohto¹, Kazuhiro Iwama³, Takeshi Mizuguchi³, Naomichi Matsumoto³ (1.Department of Pediatrics, University of Tsukuba Hospital, Ibaraki, Japan, 2.Division of Genomic Research, Life Science Research Center, Gifu University, Gifu, Japan., 3.Department of Human Genetics, Graduate School of Medicine, Yokohama City University, Yokohama, Japan)

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