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Do we need more Genome Wide Association Studies? (2021)

First Author: Menzel S

Attributed to: Identification of novel mechanisms of fetal-haemoglobin induction by common genetic variation in patients with sickle cell disease funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.3324/haematol.2021.278642

PubMed Identifier: 33832211

Publication URI: http://europepmc.org/abstract/MED/33832211

Type: Journal Article/Review

Volume: 106

Parent Publication: Haematologica

Issue: 9

ISSN: 0390-6078