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