Noushad, Muhammed <br/><br/>
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 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>2240-2993 
<br/><br/><label>Standard No.: </label>10.1007/s13760-020-01329-y  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Carrier Proteins--genetics<br/>Codon, Nonsense<br/>Female<br/>Hemangioma, Cavernous, Central Nervous System--genetics<br/>Humans<br/>Male<br/>Pedigree