Elucidating the clinical spectrum and molecular basis of HYAL2 deficiency. (2022)

First Author: Fasham J
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