4.3 Article

Prevalence of the amyloidogenic transthyretin (TTR) V122I allele in 14 333 African-Americans

Related references

Note: Only part of the references are listed.
Article Genetics & Heredity

The Genetic Ancestry of African Americans, Latinos, and European Americans across the United States

Katarzyna Bryc et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2015)

Article Medicine, General & Internal

The Amyloidogenic V122I Transthyretin Variant in Elderly Black Americans

C. Cristina Quarta et al.

NEW ENGLAND JOURNAL OF MEDICINE (2015)

Article Genetics & Heredity

Online Registry for Mutations in Hereditary Amyloidosis Including Nomenclature Recommendations

Dorota M. Rowczenio et al.

HUMAN MUTATION (2014)

Article Public, Environmental & Occupational Health

Biogeographic Ancestry, Self-Identified Race, and Admixture-Phenotype Associations in the Heart SCORE Study

Indrani Halder et al.

AMERICAN JOURNAL OF EPIDEMIOLOGY (2012)

Article Biochemistry & Molecular Biology

The first Caucasian patient with p.Val122Ile mutated-transthyretin cardiac amyloidosis treated with isolated heart transplantation

Enrico Ammirati et al.

AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS (2012)

Article Hematology

Ancestry of African Americans with sickle cell disease

Nadia Solovieff et al.

BLOOD CELLS MOLECULES AND DISEASES (2011)

Article Multidisciplinary Sciences

A map of human genome variation from population-scale sequencing

David Altshuler et al.

NATURE (2010)

Letter Cardiac & Cardiovascular Systems

Transthyretin V122I in African Americans with congestive heart failure

J Buxbaum et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2006)

Article Biochemistry & Molecular Biology

A prospective evaluation of the transthyretin Ile122 allele frequency in an African-American population

T Yamashita et al.

AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS (2005)

Article Medicine, General & Internal

Prevalence of hemochromatosis-related symptoms among individuals with mutations in the HFE gene

J Waalen et al.

MAYO CLINIC PROCEEDINGS (2002)

Article Multidisciplinary Sciences

The V122I cardiomyopathy variant of transthyretin increases the velocity of rate-limiting tetramer dissociation, resulting in accelerated amyloidosis

X Jiang et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)

Article Biochemistry & Molecular Biology

Cardiac amyloidosis associated with the transthyretin Ile122 mutation in a Caucasian family

KH Asl et al.

AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS (2001)

Article Biochemistry & Molecular Biology

Transthyretin isoleucine-122 mutation in African and American blacks

I Afolabi et al.

AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION (2000)