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Gelsolin-related amyloidosis. Identification of the amyloid protein in Finnish hereditary amyloidosis as a fragment of variant gelsolin.

The Finnish type of familial amyloidosis is a systemic disease characterized by progressive cranial neuropathy, corneal lattice dystrophy, and distal sensimotor neuropathy. Amyloid fibrils were isolated from the kidney and heart of a patient with Finnish amyloidosis. After solubilization, the amyloi...

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Bibliografische gegevens
Hoofdauteur: Maury, C P
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 1991
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC295133/
https://ncbi.nlm.nih.gov/pubmed/1849145
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