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AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis. (2017)

First Author: Andreoletti G

Attributed to: CELL SURFACE EXPRESSION OF ACID SENSITIVE K2P CHANNELS: DISSECTING THE ENDOCYTIC AND RECYCLING PATHWAYS funded by BBSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2016-104100

PubMed Identifier: 27811305

Publication URI: http://europepmc.org/abstract/MED/27811305

Type: Journal Article/Review

Volume: 54

Parent Publication: Journal of medical genetics

Issue: 4

ISSN: 0022-2593