Novel mutation of the Notch3 gene in a Japanese patient with CADASIL.

Oki, K; Nagata, E; Ishiko, A; Shimizu, A; Tanaka, K; Takahashi, K; Tabira, T; Katayama, T; Suzuki, N

Oki, K; Nagata, E; Ishiko, A; Shimizu, A; Tanaka, K; Takahashi, K; Tabira, T; Katayama, T; Suzuki, N.

Affiliation

Oki K; Department of Neurology, Keio University School of Medicine, Tokyo, Japan. di045006@sc.itc.keio.ac.jp

Eur J Neurol ; 14(4): 464-6, 2007 Apr.

Article in En | MEDLINE | ID: mdl-17389000

Subject(s)

CADASIL/genetics; Mutation, Missense; Receptors, Notch/genetics; Adult; Asian People; Brain/pathology; CADASIL/diagnosis; CADASIL/physiopathology; Diagnosis, Differential; Female; Humans; Magnetic Resonance Angiography; Magnetic Resonance Imaging; Male; Meniere Disease/diagnosis; Meniere Disease/genetics; Meniere Disease/pathology; Meniere Disease/physiopathology; Microscopy, Electron, Transmission; Pedigree; Receptor, Notch3; Skin/pathology; Tinnitus/physiopathology; Vertigo/physiopathology

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Collection: 01-internacional Database: MEDLINE Main subject: Mutation, Missense / CADASIL / Receptors, Notch Type of study: Diagnostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Eur J Neurol Journal subject: NEUROLOGIA Year: 2007 Document type: Article Affiliation country: Japan Country of publication: United kingdom

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