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Human phenotypes caused by PIEZO1 mutations; one gene, two overlapping phenotypes? (2018)

First Author: Martin-Almedina S

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/10.1113/jp275718

PubMed Identifier: 29331020

Publication URI: http://europepmc.org/abstract/MED/29331020

Type: Journal Article/Review

Volume: 596

Parent Publication: The Journal of physiology

Issue: 6

ISSN: 0022-3751