Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN)

Neurology

Volumn 70, Issue 18, 2008, Pages 1623-1629

  Kurian, M A ^a,b   Morgan, N V ^b   MacPherson, L ^a   Foster, K ^a   Peake, D ^a   Gupta, R ^a   Philip, S G ^a   Hendriksz, C ^a   Morton, J E V ^c   Kingston, H M ^d   Rosser, E M ^e   Wassmer, E ^a   Gissen, P ^b   Maher, E R ^b,c  

^a BIRMINGHAM CHILDREN S HOSPITAL   (United Kingdom)

^b UNIVERSITY DEPARTMENT OF MEDICINE   (United Kingdom)

^c BIRMINGHAM WOMEN S HOSPITAL   (United Kingdom)

^d CMMC NHS Trust

^e GREAT ORMOND STREET HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BULBAR PARALYSIS; CEREBELLAR ATAXIA; CEREBELLUM ATROPHY; COGNITION; COMPUTER ASSISTED TOMOGRAPHY; CONTROLLED STUDY; CORPUS CALLOSUM; DYSTONIA; GENE; GENE MUTATION; GENETIC POLYMORPHISM; GLIOSIS; GLOBUS PALLIDUS; HUMAN; MOLECULAR GENETICS; MOTOR PERFORMANCE; MUSCLE HYPOTONIA; NERVE DEGENERATION; NUCLEAR MAGNETIC RESONANCE IMAGING; OPTIC NERVE ATROPHY; PHENOTYPE; PLA2G6 GENE; PRIORITY JOURNAL; SPASTICITY; STRABISMUS; SUBSTANTIA NIGRA;

EID: 42949158281     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000310986.48286.8e     Document Type: Article

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