No mutations in hnRNPA1 and hnRNPA2B1 in Dutch patients with amyotrophic lateral sclerosis, frontotemporal dementia, and inclusion body myopathy. [electronic resource]
Producer: 20141208Description: 1956.e9-1956.e11 p. digitalISSN:- 1558-1497
- Adult
- Aged
- Aged, 80 and over
- Amyotrophic Lateral Sclerosis -- genetics
- Cohort Studies
- Female
- Frontotemporal Dementia -- genetics
- Genetic Association Studies
- Heterogeneous Nuclear Ribonucleoprotein A1
- Heterogeneous-Nuclear Ribonucleoprotein Group A-B -- genetics
- Humans
- Male
- Middle Aged
- Mutation
- Myositis, Inclusion Body -- genetics
- Netherlands
- Osteitis Deformans -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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