📣 Try out the NEW Gateway to Research and let us know what you think.

We're looking for users to test the new service during August and September and share their feedback. Express your interest by completing this short form.

Editorial: Molecular Mechanisms of Heritable Connective Tissue Disorders. (2022)

First Author: Malfait F

Attributed to: Pathomolecular mechanisms of intracerebral haemorrhage: functional analysis of collagen IV variants. funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.3389/fgene.2022.866665

PubMed Identifier: 35571027

Publication URI: http://europepmc.org/abstract/MED/35571027

Type: Journal Article/Review

Volume: 13

Parent Publication: Frontiers in genetics

ISSN: 1664-8021