(PDF) Next-Generation-Sequencing-Based Identification of

Next-Generation-Sequencing-Based Identification of Familial Hypercholesterolemia-Related Mutations in Subjects With Increased LDL–C Levels in a Latvian Population

BMC Medical Genetics - United Kingdom

doi 10.1186/s12881-015-0230-x

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Date

September 28, 2015

Authors

Ilze Radovica-Spalvina

Publisher

Springer Science and Business Media LLC

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Next-Generation-Sequencing-Based Identification of Familial Hypercholesterolemia-Related Mutations in Subjects With Increased LDL–C Levels in a Latvian Population

BMC Medical Genetics - United Kingdom

doi 10.1186/s12881-015-0230-x

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Identification of TAZ Mutations in Pediatric Patients With Cardiomyopathy by Targeted Next-Generation Sequencing in a Chinese Cohort

“Next Generation Sequencing Identifies Mutations in GNPTG Gene as a Cause of Familial Form of Scleroderma-Like Disease”

Analysis of HDL-microRNA Panel in Heterozygous Familial Hypercholesterolemia Subjects With LDL Receptor Null or Defective Mutation

Identification of Novel USH2A Mutations in Patients With Autosomal Recessive Retinitis Pigmentosa via Targeted Next‑generation Sequencing

ApoB Metabolism in Familial Hypercholesterolemia. Inconsistencies With the LDL Receptor Paradigm

A Chinese Homozygote of Familial Hypercholesterolemia: Identification of a Novel C263R Mutation in the LDL Receptor Gene

Next Generation Sequencing in Synovial Sarcoma Reveals Novel Gene Mutations

Coupling Chemical Mutagenesis to Next Generation Sequencing for the Identification of Drug Resistance Mutations in Leishmania

Identification of Novel GNAS Mutations in Intramuscular Myxoma Using Next-Generation Sequencing With Single-Molecule Tagged Molecular Inversion Probes