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

Noushad, Muhammed

A British family with familial cerebral cavernous malformation due to a rare mutation of the CCM2 gene. [electronic resource] - Acta neurologica Belgica Oct 2020 - 1227-1229 p. digital

Publication Type: Case Reports; Letter

2240-2993

10.1007/s13760-020-01329-y doi


Adult
Carrier Proteins--genetics
Codon, Nonsense
Female
Hemangioma, Cavernous, Central Nervous System--genetics
Humans
Male
Pedigree