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A British family with familial cerebral cavernous malformation due to a rare mutation of the CCM2 gene
Noushad, Muhammed, Bhattacharjee, Shakya, Weatherby, Stuart J., Whitefield, PeterLanguage:
english
Journal:
Acta Neurologica Belgica
DOI:
10.1007/s13760-020-01329-y
Date:
March, 2020
File:
PDF, 566 KB
english, 2020