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S Zuchner

Showing results (1-10 of 4) with videos related to

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Bioinformatics (Oxford, England)|September 24, 2010
SeqEM: an adaptive genotype-calling approach for next-generation sequencing studiesE R Martin, D D Kinnamon, M A Schmidt, et al.
Neurologia|April 27, 2026
Long-term response to aminopyridines in a cohort of patients with ataxia associated with downbeat nystagmus due to the FGF14 GAA expansionE Muñoz, M De la Cruz-Puebla, D Pellerin, et al.
Clinical Genetics|March 16, 2017
PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegiaB Ozes, N Karagoz, R Schüle, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 29, 2014
CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysisV Fridman, B Bundy, M M Reilly, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Bioinformatics (Oxford, England)|September 24, 2010
SeqEM: an adaptive genotype-calling approach for next-generation sequencing studiesE R Martin, D D Kinnamon, M A Schmidt, et al.
Neurologia|April 27, 2026
Long-term response to aminopyridines in a cohort of patients with ataxia associated with downbeat nystagmus due to the FGF14 GAA expansionE Muñoz, M De la Cruz-Puebla, D Pellerin, et al.
Clinical Genetics|March 16, 2017
PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegiaB Ozes, N Karagoz, R Schüle, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 29, 2014
CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysisV Fridman, B Bundy, M M Reilly, et al.
Pageof 1