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Translating multiscale research in rare disease. (2024)

First Author: Hooper KM

Attributed to: Congenital Anomalies - Patient-led Functional Genomics funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1242/dmm.052009

PubMed Identifier: 38982973

Publication URI: http://europepmc.org/abstract/MED/38982973

Type: Journal Article/Review

Volume: 17

Parent Publication: Disease models & mechanisms

Issue: 6

ISSN: 1754-8403