Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions. [electronic resource]
Producer: 20151019Description: 2658.e1-2658.e5 p. digitalISSN:- 1558-1497
- Aged
- Amyotrophic Lateral Sclerosis -- complications
- C9orf72 Protein
- Cohort Studies
- Female
- France
- Frontotemporal Lobar Degeneration -- complications
- Genetic Association Studies
- Genotype
- Humans
- Intercellular Signaling Peptides and Proteins -- genetics
- Italy
- Male
- Membrane Proteins -- genetics
- Middle Aged
- Mutation
- Nerve Tissue Proteins -- genetics
- Polymorphism, Genetic
- Progranulins
- Proteins -- genetics
- Trinucleotide Repeat Expansion -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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