A genealogical and clinical study of the phenotypical variation within the Swedish transthyretin His88Arg (p. His108Arg) amyloidosis family-Reference-Cited by-同舟云学术

A genealogical and clinical study of the phenotypical variation within the Swedish transthyretin His88Arg (p. His108Arg) amyloidosis family

Published:2015-04 Issue:4 Volume:58 Page:211-215
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Hellman Urban,Lundgren Hans-Erik,Westermark Per,Stafberg Christina,Nahi Hareth,Tachlinski Sascha,Guggi Michael,Flogegård Max,Hamid Mehmet,Escher Stefan A.,Suhr Ole B.

Funder

Swedish Heart-Lung Foundation

Umeå University Hospital

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

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3. Oculoleptomeningeal amyloidosis in a large kindred with a new transthyretin variant Tyr69His;Blevins;Neurology,2003

4. Transthyretin Ile84Thr is associated with familial amyloid polyneuropathy;Booth;Hum Mutat,2000

5. Synergy of combined doxycycline/TUDCA treatment in lowering Transthyretin deposition and associated biomarkers: studies in FAP mouse models;Cardoso;J Transl Med,2010

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