Clinical and electrophysiological correlates of TTRala71 amyloid neuropathy

The familial amyloidotic polyneuropathies (FAP) are autosomal dominant, length-dependent, axonal neuropathies first described in Portugal in 19581. They were later shown to be heterogeneous, resulting from tissue deposition of abnormal variants of physiological proteins, including transthyretin (TTR), apolipoprotein-A1 and gelsolin1,2 […] Clinical and electrophysiological correlates of TTRala71 amyloid neuropathy