Associated Papers
FAM91A1-TBC1D23 complex structure reveals human genetic variations susceptible for PCH.
Zhao L et al.
Proceedings of the National Academy of Sciences of the United States of America, 2023
Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar Hypoplasia.
Marin-Valencia I et al.
American Journal of Human Genetics, 2017
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