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Koichi Furakawa Selected Research

autosomal recessive Spastic paraplegia 26

9/2022Functional validation of novel variants in B4GALNT1 associated with early-onset complex hereditary spastic paraplegia with impaired ganglioside synthesis.

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Koichi Furakawa Research Topics

Disease

1autosomal recessive Spastic paraplegia 26
09/2022
1Hereditary Spastic Paraplegia
09/2022
1Rare Diseases (Rare Disease)
09/2022

Drug/Important Bio-Agent (IBA)

1GangliosidesIBA
09/2022