Clinical and Molecular Aspects of Senataxin Mutations in Amyotrophic Lateral Sclerosis 4. [electronic resource]
Producer: 20200727Description: 547-555 p. digitalISSN:- 1531-8249
- Absorptiometry, Photon
- Adipose Tissue -- diagnostic imaging
- Adult
- Aged
- Aged, 80 and over
- Amyotrophic Lateral Sclerosis -- diagnostic imaging
- Blotting, Western
- Creatine Kinase -- metabolism
- Creatinine -- metabolism
- DNA Helicases -- genetics
- Electromyography
- Female
- Fibroblasts
- Humans
- Induced Pluripotent Stem Cells
- Infant
- Lower Extremity -- diagnostic imaging
- Magnetic Resonance Imaging
- Male
- Middle Aged
- Multifunctional Enzymes -- genetics
- Muscle, Skeletal -- diagnostic imaging
- Mutation
- Neural Conduction
- R-Loop Structures -- genetics
- RNA Helicases -- genetics
- RNA, Messenger
- Upper Extremity -- diagnostic imaging
- Young Adult
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Publication Type: Journal Article; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
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