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Volumn 91, Issue 2, 2011, Pages 201-203

Hereditary gelsolin amyloidosis: A new japanese case with cutis laxa as a diagnostic clue

Author keywords

[No Author keywords available]

Indexed keywords

AGED; AMYLOIDOSIS; ARTICLE; CASE REPORT; CLINICAL FEATURE; CUTIS LAXA; DNA DETERMINATION; ELASTIC FIBER; ELECTROMYOGRAPHY; HEREDITARY GELSOLIN AMYLOIDOSIS; HUMAN; IMMUNOHISTOCHEMISTRY; JAPANESE; MALE; PIGMENTATION; PRIORITY JOURNAL; PURPURA; SCAR;

EID: 79952418068     PISSN: 00015555     EISSN: None     Source Type: Journal    
DOI: 10.2340/00015555-1011     Document Type: Article
Times cited : (7)

References (10)
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  • 2
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  • 3
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    • Postmortem pathological findings in a Japanese patient with familial amyloidosis, Finnish type (FAF)
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  • 4
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    • Lattice corneal dystrophy type II associated with familial amyloid polyneuropathy type IV
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  • 6
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    • Haplotype analysis in gelsolin-related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and Japan
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  • 8
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.