Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia

Human Molecular Genetics

Volumn 23, Issue 18, 2014, Pages 4859-4874

  Pérez Brangulí, Francesc ^a   Mishra, Himanshu K ^a   Prots, Iryna ^a   Havlicek, Steven ^a   Kohl, Zacharias ^a   Saul, Domenica ^a   Rummel, Christine ^a   Dorca Arevalo, Jonatan ^b   Regensburger, Martin ^a   Graef, Daniela ^a   Sock, Elisabeth ^a   Blasi, Juan ^b   Groemer, Teja W ^a   Schlötzer Schrehardt, Ursula ^a   Winkler, Jürgen ^a   Winner, Beate ^a  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

^b UNIVERSITY OF BARCELONA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN; SPG11 PROTEIN, HUMAN; SPG11 PROTEIN, MOUSE; TUBULIN;

ANIMAL; C57BL MOUSE; CELL CULTURE; CYTOLOGY; FOREBRAIN; GENE SILENCING; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; METABOLISM; MOUSE; NERVE CELL; NERVE FIBER; PATHOLOGY; PLURIPOTENT STEM CELL;

ANIMALS; AXONS; CELLS, CULTURED; GENE KNOCKDOWN TECHNIQUES; HUMANS; MICE; MICE, INBRED C57BL; NEURONS; PLURIPOTENT STEM CELLS; PROSENCEPHALON; PROTEINS; SPASTIC PARAPLEGIA, HEREDITARY; TUBULIN;

EID: 84906836993     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddu200     Document Type: Article

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