Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions.

Lattante, Serena

Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions. [electronic resource] - Neurobiology of aging Nov 2014 - 2658.e1-2658.e5 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1558-1497

10.1016/j.neurobiolaging.2014.06.023 doi


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