- The First Korean Family With Hereditary Gelsolin Amyloidosis Caused by p.D214Y Mutation in the GSN Gene
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Park KJ, Park JH, Park JH, Cho EB, Kim BJ, Kim JW
- KMID: 2373537
- Ann Lab Med.
- 2016 May;36(3):259-262.
- doi: 10.3343/alm.2016.36.3.259
Hereditary gelsolin amyloidosis (HGA) is an autosomal dominant hereditary disease characterized by corneal lattice dystrophy, peripheral neuropathy, and cutis laxa. So far, no Korean patients with HGA have been reported.... -
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