hCALCRL mutation causes autosomal recessive nonimmune hydrops fetalis with lymphatic dysplasia. (2018)

First Author: Mackie DI
Attributed to:  Addressing the architecture, dynamics and activation mechanism of the CGRP receptor funded by BBSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1084/jem.20180528

PubMed Identifier: 30115739

Publication URI: http://europepmc.org/abstract/MED/30115739

Type: Journal Article/Review

Volume: 215

Parent Publication: The Journal of experimental medicine

Issue: 9

ISSN: 0022-1007