Skip to main navigation
Skip to search
Skip to main content
University of Bristol Home
Help & Terms of Use
Home
Profiles
Research units
Research Outputs
Projects
Student theses
Datasets
Activities
Prizes
Facilities/Equipment
Search by expertise, name or affiliation
Molecular mechanism by which the E325K mutation of human KLF1 causes a severe dyserythropoietic anemia, utilising a novel model system of RBC disease
Frayne, Jan
(Principal Investigator)
School of Biochemistry
Overview
Project Details
Status
Finished
Effective start/end date
1/05/18
→
5/04/22
View all
View less