Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics

Human Molecular Genetics

Volumn 11, Issue 2, 2002, Pages 153-163

  Errico, Alessia ^a   Ballabio, Andrea ^a   Rugarli, Elena I ^a,b  

^a UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^b TELETHON INSTITUTE OF GENETICS AND MEDICINE TIGEM   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; MICROTUBULE PROTEIN; SPASTIN;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CELL TYPE; CONTROLLED STUDY; CYTOSKELETON; ENZYME ACTIVITY; GENETIC CODE; GENETIC TRANSFECTION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; LEG MUSCLE; MICROTUBULE ASSEMBLY; MISSENSE MUTATION; MUSCLE WEAKNESS; NERVE FIBER DEGENERATION; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DEFECT; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; PYRAMIDAL TRACT; SPASTICITY;

ANIMALIA; ASTER;

EID: 0037081740     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/11.2.153     Document Type: Article

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