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Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function. (2024)

First Author: Alpaslan M

Attributed to: Deep phenotyping to improve understanding of causal mechanisms and underlying gene mutations in primary lymphoedema and lymphatic malformations funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddae060

PubMed Identifier: 38676400

Publication URI: http://europepmc.org/abstract/MED/38676400

Type: Journal Article/Review

Volume: 33

Parent Publication: Human molecular genetics

Issue: 14

ISSN: 0964-6906