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NTIS 바로가기Annals of clinical neurophysiology : ACN, v.24 no.2, 2022년, pp.90 - 92
Kang, Minsung (Department of Neurology, Kyungpook National University Chilgok Hospital) , Shin, Jin-Hong (Department of Neurology, Pusan National University Yangsan Hospital) , Kim, Dae-Seong (Department of Neurology, Pusan National University Yangsan Hospital)
AGel amyloidosis is an autosomal dominantly inherited disease caused by a GSN mutation, and affected patients typically present with the clinical triad of corneal lattice dystrophy, progressive cranial neuropathy, and cutis laxa. We report a Korean family with AGel amyloidosis with predominant manif...
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