Asp58Ala is the Predominant Mutation of the TTR Gene in Korean Patients with Hereditary Transthyretin‐Related Amyloidosis

Publisher： John Wiley & Sons Inc

E-ISSN： 1469-1809|79|2|99-107

ISSN： 0003-4800

Source： ANNALS OF HUMAN GENETICS, Vol.79, Iss.2, 2015-03, pp. : 99-107

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