Elucidating the clinical spectrum and molecular basis of HYAL2 deficiency. (2022)
Attributed to:
Precision Medicine Exeter Innovation Platform (PMEI Platform)
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.gim.2021.10.014
PubMed Identifier: 34906488
Publication URI: http://europepmc.org/abstract/MED/34906488
Type: Journal Article/Review
Volume: 24
Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics
Issue: 3
ISSN: 1098-3600