Abstract
Phenotypic heterogeneity and evidence of a founder effect associated with <i>G6<scp>PC</scp>3</i> mutations in patients with severe congenital neutropenia
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
