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Björkenheim, A. et al. (2020). Hereditary transthyretin amyloidosis caused by the rare Phe33Leu mutation. BMJ case reports. 13 (1), p. . [Online].
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Björkenheim, A. et al. (2020). Hereditary transthyretin amyloidosis caused by the rare Phe33Leu mutation. BMJ case reports. 13 (1), p. . [Online].