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Kosuke Nakashima

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Movement Disorders : Official Journal of the Movement Disorder Society|February 3, 2018
A homozygous loss-of-function mutation in PDE2A associated to early-onset hereditary choreaVincenzo Salpietro, Belen Perez-Dueñas, Kosuke Nakashima, et al.
American Journal of Human Genetics|April 9, 2016
De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal LesionsNiccolò E Mencacci, Erik-Jan Kamsteeg, Kosuke Nakashima, et al.
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Showing results (51-60 of 52) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 52 results.
Movement Disorders : Official Journal of the Movement Disorder Society|February 3, 2018
A homozygous loss-of-function mutation in PDE2A associated to early-onset hereditary choreaVincenzo Salpietro, Belen Perez-Dueñas, Kosuke Nakashima, et al.
American Journal of Human Genetics|April 9, 2016
De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal LesionsNiccolò E Mencacci, Erik-Jan Kamsteeg, Kosuke Nakashima, et al.
Pageof 6