ALSFTD - What does ALSFTD stand for? The Free Dictionary
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.