OPA1, associated with autosomal dominant optic atrophy, is widely expressed in the human brain

Acta Neuropathologica

Volumn 109, Issue 4, 2005, Pages 393-399

  Bette, Stefanie ^a   Schlaszus, Holger ^b   Wissinger, Bernd ^a   Meyermann, Richard ^b   Mittelbronn, Michel ^b  

^a UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

^b UNIVERSITY OF TÜBINGEN   (Germany)

Author keywords

Astrocytes; Human brain; Neurons; OPA1 protein; Optic atrophy

Indexed keywords

GENE PRODUCT; PROTEIN OPA1; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ANTIBODY LABELING; ARTICLE; AUTOSOMAL DOMINANT OPTIC ATROPHY; CARBOXY TERMINAL SEQUENCE; CLINICAL FEATURE; DISEASE ASSOCIATION; FRONTAL CORTEX; GENE MUTATION; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; MOTOR CORTEX; NEUROPATHOLOGY; NONHUMAN; NORTHERN BLOTTING; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; PURKINJE CELL; RAT; RAT STRAIN; WESTERN BLOTTING;

EID: 18344378456     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00401-004-0970-8     Document Type: Article

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