Systemic AA amyloidosis as a unique manifestation of a combined mutation of TNFRSF1A and MEFV genes
about
Piedmont and Aosta Valley inter-regional network in the context of the Italian National Network for rare diseases.Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.Evidence of digenic inheritance in autoinflammation-associated genes.Immunological Rare Diseases.
P2860
Systemic AA amyloidosis as a unique manifestation of a combined mutation of TNFRSF1A and MEFV genes
description
article
@en
im März 2013 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в березні 2013
@uk
name
Systemic AA amyloidosis as a u ...... ion of TNFRSF1A and MEFV genes
@en
Systemic AA amyloidosis as a u ...... ion of TNFRSF1A and MEFV genes
@nl
type
label
Systemic AA amyloidosis as a u ...... ion of TNFRSF1A and MEFV genes
@en
Systemic AA amyloidosis as a u ...... ion of TNFRSF1A and MEFV genes
@nl
prefLabel
Systemic AA amyloidosis as a u ...... ion of TNFRSF1A and MEFV genes
@en
Systemic AA amyloidosis as a u ...... ion of TNFRSF1A and MEFV genes
@nl
P2093
P2860
P1433
P1476
Systemic AA amyloidosis as a u ...... ion of TNFRSF1A and MEFV genes
@en
P2093
Dario Roccatello
Edoardo Errichiello
Gianna Mazzucco
Giovanni B. Binello
Giovanni G. Battaglia
Oana M. Mereuta
Simone Baldovino
P2860
P304
P356
10.3109/13506129.2013.775119
P577
2013-03-06T00:00:00Z