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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Steven Froelich

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Brain : a Journal of Neurology|August 30, 2023

SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysisArthur Stefanski, Eduardo Pérez-Palma, Tobias Brünger, et al.

Nature Medicine|July 3, 2019

Allele-selective transcriptional repression of mutant HTT for the treatment of Huntington's diseaseBryan Zeitler, Steven Froelich, Kimberly Marlen, et al.

Medrxiv : the Preprint Server for Health Sciences|March 13, 2026

Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant ClassificationTobias Brünger, Ilona Krey, Suyeon Kim, et al.

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Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 13 results.

Brain : a Journal of Neurology|August 30, 2023

SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysisArthur Stefanski, Eduardo Pérez-Palma, Tobias Brünger, et al.

Nature Medicine|July 3, 2019

Allele-selective transcriptional repression of mutant HTT for the treatment of Huntington's diseaseBryan Zeitler, Steven Froelich, Kimberly Marlen, et al.

Medrxiv : the Preprint Server for Health Sciences|March 13, 2026

Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant ClassificationTobias Brünger, Ilona Krey, Suyeon Kim, et al.

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