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The V122I mutation in hereditary transthyretin-mediated amyloidosis is significantly associated with an increased incidence of polyneuropathy

Document Type

Journal

Author

Parker, M. M.; Damrauer, S. M.; Erbe, D.; Aldinc, E.; Ticau, S.; Flynn-Carroll, A.; Deaton, A. M.; Ward, L. D.; Rader, D. J.; Fitzgerald, K.; Vaishnaw, A. K.; Hinkle, G.; Nioi, P.

Source

EUROPEAN HEART JOURNAL; NOV 2020, 41 p3143-p3143, 1p. Supplement: 2

Subject

Language

English

ISSN

15229645

Online Access

Full Text (Oxford University Press) Full Text (OUP Near Archive) Web of Science JCR 저널정보 Find it@PNU

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