Familial versus sporadic cavernous malformations: differences in developmental venous anomaly association and lesion phenotype. [electronic resource]
Producer: 20100423Description: 377-82 p. digitalISSN:- 1936-959X
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Cerebral Veins -- abnormalities
- Child
- Child, Preschool
- Female
- Genetic Predisposition to Disease -- epidemiology
- Hemangioma, Cavernous, Central Nervous System -- epidemiology
- Humans
- Infant
- KRIT1 Protein
- Magnetic Resonance Imaging
- Male
- Microtubule-Associated Proteins -- genetics
- Middle Aged
- Phenotype
- Proto-Oncogene Proteins -- genetics
- Retrospective Studies
- Risk Factors
- Young Adult
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Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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