Wordt geladen...
Novel KRIT1/CCM1 and MGC4607/CCM2 Gene Variants in Chinese Families With Cerebral Cavernous Malformations
Familial cerebral cavernous malformations (CCMs) are autosomal dominant disorders characterized by hemorrhagic strokes, recurrent headache, epilepsy, and focal neurological deficits. Genetic variants in KRIT1/CCM1, MGC4607/CCM2, and PDCD10/CCM3 genes contribute to CCMs. The clinical information of t...
Bewaard in:
| Gepubliceerd in: | Front Neurol |
|---|---|
| Hoofdauteurs: | , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Frontiers Media S.A.
2018
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6308150/ https://ncbi.nlm.nih.gov/pubmed/30622508 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2018.01128 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|