SPG11 - The most common type of recessive spastic paraplegia in Norway?

Acta Neurologica Scandinavica

Volumn 117, Issue SUPPL. 188, 2008, Pages 46-50

  Erichsen, A K ^a   Stevanin, G ^b,c   Denora, P ^b,c   Brice, A ^b,c   Tallaksen, C M E ^a,d  

^a ULLEVÅL UNIVERSITY HOSPITAL   (Norway)

^b INSERM   (France)

^c PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^d UNIVERSITY OF OSLO   (Norway)

Author keywords

Corpus callosum hypoplasia; Hereditary spastic paraplegia; Neurodegenerative disorder; Spatacsin; SPG11

Indexed keywords

NEUROLEPTIC AGENT; PROTEIN; SPG11 PROTEIN, HUMAN;

ADULT; ANAMNESIS; ARTICLE; BLOOD EXAMINATION; BRAIN ATROPHY; CASE REPORT; CEREBELLUM ATROPHY; CEREBROSPINAL FLUID ANALYSIS; CLINICAL FEATURE; COGNITIVE DEFECT; CORPUS CALLOSUM; DISEASE COURSE; DYSARTHRIA; ELECTROMYOGRAPHY; FACIAL NERVE PARALYSIS; FEMALE; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN TISSUE; MALE; MUSCLE BIOPSY; NEUROGRAPHY; NEUROLOGIC EXAMINATION; NORWAY; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; PROTEIN ANALYSIS; PYRAMIDAL SIGN; RECESSIVE GENE; RECESSIVE INHERITANCE; SPG 11 GENE; VIBRATION SENSE; GENETICS; MENTAL DEFICIENCY; MIDDLE AGED; PATHOLOGY; PEDIGREE; PSYCHOLOGICAL ASPECT;

ADULT; CORPUS CALLOSUM; FEMALE; GENES, RECESSIVE; HUMANS; MALE; MENTAL RETARDATION; MIDDLE AGED; NORWAY; PEDIGREE; PHENOTYPE; PROTEINS; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 42649088751     PISSN: 00016314     EISSN: 16000404     Source Type: Journal    
DOI: 10.1111/j.1600-0404.2008.01031.x     Document Type: Article

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