Add to ORKGDanish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type
Mutations in the gelsolin protein are responsible for a rare conformational disease known as AGel am...
Familial amyloidosis of the Finnish type (FAF) is an autosomal dominant form of systemic amyloidosis...
Copyright © 2015 Isabel Tavares et al. This is an open access article distributed under the Creative...
The Finnish type of familial amyloidosis is a systemic disease characterized by progressive cranial ...
Finnish gelsolin amyloidosis (AGel amyloidosis) is an autosomal dominantly inherited systemic disord...
AbstractThe amyloid protein in Finnish hereditary amyloidosis is a fragment of the actin-filament bi...
Gelsolin amyloidosis typically presents with corneal lattice dystrophy and is most frequently associ...
Finnish-type familial amyloidosis (FAF) is a rare hereditary systemic amyloidosis that mainly exhi-b...
AbstractFamilial amyloidosis, Finnish type is caused by a single base mutation in gelsolin, an actin...
Gelsolin (GSN) variants have been implicated in amyloidosis of the Finnish type. This case series re...
Hereditary gelsolin amyloidosis is a rare subtype of hereditary systemic amyloidosis. An old male pr...
AbstractGelsolin, an actin-modulating protein, derived from a single gene exists in intracellular an...
AbstractAmyloid fibrils were isolated from the kidney of a patient with Finnish hereditary amyloidos...
AbstractBackground:Normally, gelsolin functions in plasma as part of the actin-scavenging system to ...
Background Hereditary gelsolin (AGel) amyloidosis is an autosomal dominantly inherited systemic amyl...
Mutations in the gelsolin protein are responsible for a rare conformational disease known as AGel am...
Familial amyloidosis of the Finnish type (FAF) is an autosomal dominant form of systemic amyloidosis...
Copyright © 2015 Isabel Tavares et al. This is an open access article distributed under the Creative...
The Finnish type of familial amyloidosis is a systemic disease characterized by progressive cranial ...
Finnish gelsolin amyloidosis (AGel amyloidosis) is an autosomal dominantly inherited systemic disord...
AbstractThe amyloid protein in Finnish hereditary amyloidosis is a fragment of the actin-filament bi...
Gelsolin amyloidosis typically presents with corneal lattice dystrophy and is most frequently associ...
Finnish-type familial amyloidosis (FAF) is a rare hereditary systemic amyloidosis that mainly exhi-b...
AbstractFamilial amyloidosis, Finnish type is caused by a single base mutation in gelsolin, an actin...
Gelsolin (GSN) variants have been implicated in amyloidosis of the Finnish type. This case series re...
Hereditary gelsolin amyloidosis is a rare subtype of hereditary systemic amyloidosis. An old male pr...
AbstractGelsolin, an actin-modulating protein, derived from a single gene exists in intracellular an...
AbstractAmyloid fibrils were isolated from the kidney of a patient with Finnish hereditary amyloidos...
AbstractBackground:Normally, gelsolin functions in plasma as part of the actin-scavenging system to ...
Background Hereditary gelsolin (AGel) amyloidosis is an autosomal dominantly inherited systemic amyl...
Mutations in the gelsolin protein are responsible for a rare conformational disease known as AGel am...
Familial amyloidosis of the Finnish type (FAF) is an autosomal dominant form of systemic amyloidosis...
Copyright © 2015 Isabel Tavares et al. This is an open access article distributed under the Creative...