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Papers of the Week

Home / Publications / Pain Research Forum / Papers of the Week / A British family with familial cerebral cavernous malformation due to a rare mutation of the CCM2 gene.

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2020 Mar 13


Acta Neurol Belg


http://www.ncbi.nlm.nih.gov/pubmed/32170606?dopt=Abstract

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

Authors

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.
Read This Paper