Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility.

Blood

Genetic Epidemiology Branch, Division of Cancer Epidemiology and Genetics.

Published: November 2016

Download full-text PDF	Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095758	PMC
http://dx.doi.org/10.1182/blood-2016-02-697771	DOI Listing

Publication Analysis

exome sequencing

sequencing families

families cll

cll detects

detects variant

variant integrin

integrin associated

associated disease

disease susceptibility

exome

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!