Juvenile form of Alexander disease with GFAP mutation and mitochondrial abnormality.

Nobuhara, Y; Nakahara, K; Higuchi, I; Yoshida, T; Fushiki, S; Osame, M; Arimura, K; Nakagawa, M

Nobuhara, Y; Nakahara, K; Higuchi, I; Yoshida, T; Fushiki, S; Osame, M; Arimura, K; Nakagawa, M.

Affiliation

Nobuhara Y; Department of Neurology and Gerontology, Kagoshima University Graduate School of Medical and Dental Sciences, Japan.

Neurology ; 63(7): 1302-4, 2004 Oct 12.

Article in En | MEDLINE | ID: mdl-15477559

Subject(s)

Alexander Disease/genetics; DNA, Mitochondrial/genetics; Glial Fibrillary Acidic Protein/genetics; Adult; Alexander Disease/pathology; Base Sequence; Central Nervous System/pathology; Child; Exons; Female; Humans; Magnetic Resonance Imaging; Mitochondrial Myopathies/genetics; Mitochondrial Myopathies/pathology; Muscle Fibers, Skeletal/pathology; Point Mutation; Sequence Deletion

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Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Alexander Disease / Glial Fibrillary Acidic Protein Limits: Adult / Child / Female / Humans Language: En Journal: Neurology Year: 2004 Document type: Article Affiliation country: Japan Country of publication: United States

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