Nervenheilkunde
 2019
DOI: 10.1055/s-0039-1684976
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Herausforderung hereditäre Transthyretin-Amyloidose: Ab wann ist ein Mutationsträger ein Patient? Eine longitudinale Beobachtungsstudie fraglich symptomatischer Träger der heterozygoten TTR-Mutation Val30Met

MF Dohrn
1
,
Teresa Coelho
2
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