QuickView for TTR;jsessionid=B764E6EA4711583BB8C82894D6C98508 (gene)

1. Probing the Dissociation Pathway of a Kinetically Labile Transthyretin Mutant.
2. Rare c.302C>T TTR Variant Associated with Transthyretin Amyloidosis.
3. Late-onset familial amyloidosis polyneuropathy associated with c.186G>C in transthyretin.
4. Clinical spectrum of Transthyretin amyloidogenic mutations among diverse population origins.
5. Therapeutic Strategies for Hereditary Transthyretin Amyloidosis].

There were no clinical trials for TTR;jsessionid=B764E6EA4711583BB8C82894D6C98508