32719 PDFs Review articles in ATAXIA
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32719 PDFs Review articles in ATAXIA
Genes for spinocerebellar ataxia with blindness and deafness (SCABD/SCAR3, MIM# 271250 and SCABD2)
Spinocerebellar ataxia Nature Reviews Disease Primers
New Cerebellar Ataxia, Neuropathy, Vestibular Areflexia Syndrome cases are caused by the presence of a nonsense variant in compound heterozygosity with the pathogenic repeat expansion in the RFC1 gene - Arteche‐López
Ataxia (Chapter 14) - Magnetic Resonance Imaging in Movement Disorders
Frontiers Role of Calpain-1 in Neurogenesis
32719 PDFs Review articles in ATAXIA
Characterization of Lifestyle in Spinocerebellar Ataxia Type 3 and Association with Disease Severity - Hengel - 2022 - Movement Disorders - Wiley Online Library
FXN gene methylation determines carrier status in Friedreich ataxia
Table of Contents page: Journal of Biological Chemistry
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