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Kathrin Hauser

Showing results (51-60 of 52) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|February 6, 2021
The Mutation Matters: CSF Profiles of GCase, Sphingolipids, α-Synuclein in PD<sub>GBA</sub>Stefanie Lerche, Claudia Schulte, Isabel Wurster, et al.
American Journal of Human Genetics|May 19, 2015
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaNiccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, 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 6, 2021
The Mutation Matters: CSF Profiles of GCase, Sphingolipids, α-Synuclein in PD<sub>GBA</sub>Stefanie Lerche, Claudia Schulte, Isabel Wurster, et al.
American Journal of Human Genetics|May 19, 2015
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaNiccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, et al.
Pageof 6