Novel mutation of the Notch3 gene in a Japanese patient with CADASIL. [electronic resource]
Producer: 20070613Description: 464-6 p. digitalISSN:- 1468-1331
- Adult
- Asian People
- Brain -- pathology
- CADASIL -- diagnosis
- Diagnosis, Differential
- Female
- Humans
- Magnetic Resonance Angiography
- Magnetic Resonance Imaging
- Male
- Meniere Disease -- diagnosis
- Microscopy, Electron, Transmission
- Mutation, Missense
- Pedigree
- Receptor, Notch3
- Receptors, Notch -- genetics
- Skin -- pathology
- Tinnitus -- physiopathology
- Vertigo -- physiopathology
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Publication Type: Journal Article
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