Editorial: molecular mechanisms of heritable connective tissue disorders

Malfait, F., Forlino, A., Sengle, G. and Van Agtmael, T. (2022) Editorial: molecular mechanisms of heritable connective tissue disorders. Frontiers in Genetics, 13, 866665. (doi: 10.3389/fgene.2022.866665) (PMCID:PMC9091304)

[img] Text
270783.pdf - Published Version
Available under License Creative Commons Attribution.

554kB

Abstract

No abstract available.

Item Type:Articles (Editorial)
Keywords:Genetics, extracellular matrix, heritable disorders of connective tissue, connective tissue, collagen, proteoglycans (PG), fibrillin (FBN).
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Van Agtmael, Professor Tom
Authors: Malfait, F., Forlino, A., Sengle, G., and Van Agtmael, T.
College/School:College of Medical Veterinary and Life Sciences > School of Cardiovascular & Metabolic Health
Journal Name:Frontiers in Genetics
Publisher:Frontiers Media
ISSN:1664-8021
ISSN (Online):1664-8021
Copyright Holders:Copyright © 2022 Malfait, Forlino, Sengle and Van Agtmael
First Published:First published in Frontiers in Genetics 13: 866665
Publisher Policy:Reproduced under a Creative Commons License

University Staff: Request a correction | Enlighten Editors: Update this record

Project CodeAward NoProject NamePrincipal InvestigatorFunder's NameFunder RefLead Dept
302164Collagen IV variants and their role in intracerebral haemorrhage in the general populationTom Van AgtmaelMedical Research Council (MRC)MR/R005567/1CAMS - Cardiovascular Science
300478Elucidation of molecular pathways underlying cardiac disease caused by Col4a1 mutationsTom Van AgtmaelHeart Research UK (HEARTRES)RG 2664/17/20CAMS - Cardiovascular Science