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Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type.

Familial amyloidosis, Finnish type (FAF), is an inherited form of systemic amyloidosis clinically characterized by cranial neuropathy and lattice corneal dystrophy. We have demonstrated that the protein subunit isolated from amyloid fibrils shows considerable sequence identity with gelsolin, an acti...

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Détails bibliographiques
Auteurs principaux: Ghiso, J, Haltia, M, Prelli, F, Novello, J, Frangione, B
Format: Artigo
Langue:Inglês
Publié: 1990
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1149782/
https://ncbi.nlm.nih.gov/pubmed/2176481
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