ALSFTDAmyotrophic Lateral Sclerosis with Frontotemporal Dementia
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References in periodicals archive ?
Veldink et al., "A case of ALSFTD in a large FALS pedigree with a K17I ANG mutation," Neurology, vol.
Shatunov et al., "The C9ORF72 expansion mutation is a common cause of ALSFTD in Europe and has a single founder," European Journal of Human Genetics, vol.
Gibbs et al., "A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALSFTD," Neuron, vol.