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Papers of the Week

2020 Mar 13

Acta Neurol Belg

A British family with familial cerebral cavernous malformation due to a rare mutation of the CCM2 gene.


Noushad M, Bhattacharjee S, Weatherby SJ, Whitefield P
Acta Neurol Belg. 2020 Mar 13.
PMID: 32170606.