A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy.
about
Mutant proteins as cancer-specific biomarkersIdentification of a novel proteoform of prostate specific antigen (SNP-L132I) in clinical samples by multiple reaction monitoringStructure-based analysis of A19D, a variant of transthyretin involved in familial amyloid cardiomyopathy.A prospective evaluation of the transthyretin Ile122 allele frequency in an African-American population.Asp58Ala is the predominant mutation of the TTR gene in Korean patients with hereditary transthyretin-related amyloidosis.Unfolding and aggregation of transthyretin by the truncation of 50 N-terminal amino acids.
P2860
A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy.
description
2004 nî lūn-bûn
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2004年の論文
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2004年学术文章
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2004年学术文章
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2004年学术文章
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2004年学术文章
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2004年学术文章
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2004年學術文章
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2004年學術文章
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2004年學術文章
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name
A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy.
@en
A rare transthyretin mutation
@nl
type
label
A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy.
@en
A rare transthyretin mutation
@nl
prefLabel
A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy.
@en
A rare transthyretin mutation
@nl
P2093
P2860
P1433
P1476
A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy.
@en
P2093
Martha Skinner
Masahide Yazaki
Merrill D Benson
Taro Yamashita
P2860
P356
10.1080/13506120410001682569
P577
2004-03-01T00:00:00Z