Cite
HARVARD Citation
Patel, K. et al. (2018). A case of transthyretin amyloidosis with myopathy, neuropathy, and cardiomyopathy resulting from an exceedingly rare mutation transthyretin Ala120Ser (c.418G > T, p.Ala140Ser). Amyloid. pp. 211-212. [Online].