Meningocerebrovascular amyloidosis associated with a novel transthyretin mis-sense mutation at codon 18 (TTRD18G)

American Journal of Pathology

Volumn 148, Issue 2, 1996, Pages 361-366

  Vidal, Ruben ^a   Garzuly, Ferenc ^b   Budka, Herbert ^c   Lalowski, Maciej ^a   Linke, Reinhold P ^d   Brittig, Ferenc ^b   Frangione, Blas ^a   Wisniewski, Thomas ^a  

^a NEW YORK UNIVERSITY MEDICAL CENTER   (United States)

^b Markusovszky Teaching Hospital   (Hungary)

^c MEDICAL UNIVERSITY OF VIENNA   (Austria)

^d MAX PLANCK INSTITUTE   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID; AMYLOID BETA PROTEIN; ASPARTIC ACID; CYSTATIN C; GLYCINE; PREALBUMIN;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; ATAXIA; CEREBROVASCULAR DISEASE; CODON; DEMENTIA; FEMALE; HEART DISEASE; HUMAN; HUMAN TISSUE; HUNGARY; MAJOR CLINICAL STUDY; MALE; MENINX DISORDER; MISSENSE MUTATION; PERIPHERAL NEUROPATHY; PRION; PRIORITY JOURNAL; SPASTICITY; STROKE; VASCULAR AMYLOIDOSIS;

AMINO ACID SEQUENCE; AMYLOID; BASE SEQUENCE; CEREBRAL AMYLOID ANGIOPATHY; CODON; DNA; FEMALE; GENOTYPE; HUMANS; HUNGARY; IMMUNOHISTOCHEMISTRY; MALE; MENINGES; MOLECULAR SEQUENCE DATA; PEDIGREE; POINT MUTATION; POLYMERASE CHAIN REACTION; PREALBUMIN;

EID: 0030040173     PISSN: 00029440     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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