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JMEDGENET-2015-103476
JMEDGENET-2015-103476
http://dx.doi.org/10.1136/JMEDGENET-2015-103476
Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations
P356
Q36983068-579F20C8-BF7B-41F1-B239-616F7252D01C
P356
JMEDGENET-2015-103476
http://dx.doi.org/10.1136/JMEDGENET-2015-103476