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1
J.EJPN.2013.05.003
J.EJPN.2013.05.003
http://dx.doi.org/10.1016/J.EJPN.2013.05.003
Cerebral cavernous malformation: clinical report of two families with variable phenotype associated with KRIT1 mutation.
P356
Q38117525-AC4298E4-7F01-461F-915D-5B0CC6EB7C5C
P356
J.EJPN.2013.05.003
http://dx.doi.org/10.1016/J.EJPN.2013.05.003