İstanbul Bilim Üniversitesi, Tıp Fakültesi.Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) is an autosomal dominant disorder caused by mutations of the transthyretin (TTR) gene. More than 100 different mutations of the transthyretin gene were identified worlwide, but still the first described Val30Met is the most common one.http://onlinelibrary.wiley.com/doi/10.1111/ene.12495/pd
Familial amyloid polyneuropathy (FAP) is a progressive systemic autosomal dominant disease caused by...
Familial amyloid polyneuropathy (FAP) is rare and most commonly caused by the Val30Met mutation of t...
International audienceTransthyretin familial amyloid polyneuropathies (TTR-FAPs) are autosomal domin...
PubMed ID: 27238058Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) is an autosomal d...
Transthyretin-associated familial amyloid polyneuropathy (TTR-FAP) is an unusual but life-threatenin...
Familial amyloid polyneuropathy (FAP) is a rare condition caused by mutations of the transthyretin (...
Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) is caused by gain-of-toxic-function ...
Background. Transthyretin-related familial amyloid polyneuropathy (ATTR-FAP) is a rare, progressive,...
Familial amyloidotic polyneuropathy type 1 (FAP1, MIM176300) is an autosomal dominant disease caused...
Peripheral-Nerve-Society Meeting -- JUL 08-12, 2017 -- Sitges, SPAINWOS: 000409243500128…Peripheral ...
Introduction: Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) typically arises as an...
We herein report the case of an 84-year-old woman with transthyretin (TTR) Val30Met-associated famil...
mutation.Giessen, GermanyFull list of author information is available at the end of the articlefiber...
The authors reviewed contribution of Kumamoto University group to the progress of the studies on tra...
mutation.Giessen, GermanyFull list of author information is available at the end of the articlefiber...
Familial amyloid polyneuropathy (FAP) is a progressive systemic autosomal dominant disease caused by...
Familial amyloid polyneuropathy (FAP) is rare and most commonly caused by the Val30Met mutation of t...
International audienceTransthyretin familial amyloid polyneuropathies (TTR-FAPs) are autosomal domin...
PubMed ID: 27238058Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) is an autosomal d...
Transthyretin-associated familial amyloid polyneuropathy (TTR-FAP) is an unusual but life-threatenin...
Familial amyloid polyneuropathy (FAP) is a rare condition caused by mutations of the transthyretin (...
Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) is caused by gain-of-toxic-function ...
Background. Transthyretin-related familial amyloid polyneuropathy (ATTR-FAP) is a rare, progressive,...
Familial amyloidotic polyneuropathy type 1 (FAP1, MIM176300) is an autosomal dominant disease caused...
Peripheral-Nerve-Society Meeting -- JUL 08-12, 2017 -- Sitges, SPAINWOS: 000409243500128…Peripheral ...
Introduction: Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) typically arises as an...
We herein report the case of an 84-year-old woman with transthyretin (TTR) Val30Met-associated famil...
mutation.Giessen, GermanyFull list of author information is available at the end of the articlefiber...
The authors reviewed contribution of Kumamoto University group to the progress of the studies on tra...
mutation.Giessen, GermanyFull list of author information is available at the end of the articlefiber...
Familial amyloid polyneuropathy (FAP) is a progressive systemic autosomal dominant disease caused by...
Familial amyloid polyneuropathy (FAP) is rare and most commonly caused by the Val30Met mutation of t...
International audienceTransthyretin familial amyloid polyneuropathies (TTR-FAPs) are autosomal domin...
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