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2016.6.JNS16665
2016.6.JNS16665
http://dx.doi.org/10.3171/2016.6.JNS16665
Familial occurrence of brain arteriovenous malformation: a novel ACVRL1 mutation detected by whole exome sequencing.
P356
Q48522009-A0EE25D8-DA02-488E-9043-8BA4C65B6F52
P356
2016.6.JNS16665
http://dx.doi.org/10.3171/2016.6.JNS16665