Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Rare Variants in Cardiomyopathy Genes Associated With Stress-Induced Cardiomyopathy
by
Forseth, James
, Corneveaux, Jason J.
, Richholt, Ryan
, Kalani, M. Yashar S.
, Spetzler, Robert F.
, Siniard, Ashley L.
, Nakaji, Peter
, Huentelman, Matthew J.
, Zabramski, Joseph M.
, Bruhns, Ryan
in
Adult
/ Cardiomyopathies - genetics
/ Cardiomyopathy
/ European Continental Ancestry Group
/ Exome
/ Female
/ Genetic Predisposition to Disease - genetics
/ Genetic Variation
/ High-Throughput Nucleotide Sequencing
/ Humans
/ Male
/ Neurosurgery
/ Patients
/ Stress, Physiological - genetics
/ Stress, Psychological - genetics
2016
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Rare Variants in Cardiomyopathy Genes Associated With Stress-Induced Cardiomyopathy
by
Forseth, James
, Corneveaux, Jason J.
, Richholt, Ryan
, Kalani, M. Yashar S.
, Spetzler, Robert F.
, Siniard, Ashley L.
, Nakaji, Peter
, Huentelman, Matthew J.
, Zabramski, Joseph M.
, Bruhns, Ryan
in
Adult
/ Cardiomyopathies - genetics
/ Cardiomyopathy
/ European Continental Ancestry Group
/ Exome
/ Female
/ Genetic Predisposition to Disease - genetics
/ Genetic Variation
/ High-Throughput Nucleotide Sequencing
/ Humans
/ Male
/ Neurosurgery
/ Patients
/ Stress, Physiological - genetics
/ Stress, Psychological - genetics
2016
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Rare Variants in Cardiomyopathy Genes Associated With Stress-Induced Cardiomyopathy
by
Forseth, James
, Corneveaux, Jason J.
, Richholt, Ryan
, Kalani, M. Yashar S.
, Spetzler, Robert F.
, Siniard, Ashley L.
, Nakaji, Peter
, Huentelman, Matthew J.
, Zabramski, Joseph M.
, Bruhns, Ryan
in
Adult
/ Cardiomyopathies - genetics
/ Cardiomyopathy
/ European Continental Ancestry Group
/ Exome
/ Female
/ Genetic Predisposition to Disease - genetics
/ Genetic Variation
/ High-Throughput Nucleotide Sequencing
/ Humans
/ Male
/ Neurosurgery
/ Patients
/ Stress, Physiological - genetics
/ Stress, Psychological - genetics
2016
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Rare Variants in Cardiomyopathy Genes Associated With Stress-Induced Cardiomyopathy
Journal Article
Rare Variants in Cardiomyopathy Genes Associated With Stress-Induced Cardiomyopathy
2016
Request Book From Autostore
and Choose the Collection Method
Overview
Abstract
BACKGROUND:
Stress-induced cardiomyopathy (SIC) is a poorly understood condition associated with periods of emotional and physical stress. The clinical approaches for management of SIC are supportive and reactive to patient symptoms.
OBJECTIVE:
To utilize next-generation exome sequencing to define genetic variation associated with, and potentially responsible for, this disease.
METHODS:
We performed exome sequencing of 7 white female patients with SIC. Filtering of the identified variants was performed to limit our investigation to those sequences that passed quality control criteria, were rare or novel, were determined algorithmically to have high impact on the associated protein, and were within regions of high species conservation. All variants were verified by using Sanger sequencing.
RESULTS:
Exome-sequencing analysis revealed that each patient carried predicted deleterious variants affecting known cardiomyopathy genes. In each case, the identified variant was either not previously found in public human genome data or was previously annotated in a database of clinical variants associated with cardiac dysfunction.
CONCLUSION:
Patients with SIC harbor deleterious mutations in established cardiomyopathy genes at a level higher than healthy controls. We hypothesize that patients at highest risk for SIC likely live in a compensated state of cardiac dysfunction that manifests clinically only after the myocardium is stressed. In short, we propose that SIC is another example of an occult cardiomyopathy with a distinct physiological trigger and suggest that alternative clinical approaches to these patients may be warranted.
Publisher
Oxford University Press,Copyright by the Congress of Neurological Surgeons,Wolters Kluwer Health, Inc
MBRLCatalogueRelatedBooks
Related Items
Related Items
This website uses cookies to ensure you get the best experience on our website.