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JMEDGENET-2016-104100
JMEDGENET-2016-104100
http://dx.doi.org/10.1136/JMEDGENET-2016-104100
AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis
P356
Q28975784-3D9E964D-19A6-44DD-B395-D6632AB306F5
P356
JMEDGENET-2016-104100
http://dx.doi.org/10.1136/JMEDGENET-2016-104100