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A new mutant transthyretin (Arg 10) associated with familial amyloid polyneuropathy.The Genetic Challenges and Opportunities in Advanced Heart FailureAmyloid polyneuropathy in two German-American families: a new transthyretin variant (Val 107)Hereditary renal amyloidosis with a novel variant fibrinogen.Exclusion of the gelsolin gene on 9q32-34 as the cause of familial lattice corneal dystrophy type I.A critical analysis of postulated pathogenetic mechanisms in amyloidogenesis.Long term results of heart transplantation in patients with amyloid heart disease.Apolipoprotein AI-derived pulmonary vascular amyloid in aged dogs.Pulmonary vascular amyloidosis in aged dogs. A new form of spontaneously occurring amyloidosis derived from apolipoprotein AI.Identification of a novel non-amyloidogenic transthyretin polymorphism (His 74) in the German populationArgentinian patients of European ancestry with familial amyloid polyneuropathyA new transthyretin variant (His 69) associated with vitreous amyloid in an FAP family
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on February 1991
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Inherited amyloidosis.
@en
Inherited amyloidosis.
@nl
type
label
Inherited amyloidosis.
@en
Inherited amyloidosis.
@nl
prefLabel
Inherited amyloidosis.
@en
Inherited amyloidosis.
@nl
P2860
P356
P1476
Inherited amyloidosis.
@en
P2093
P2860
P356
10.1136/JMG.28.2.73
P407
P577
1991-02-01T00:00:00Z