A novel hereditary spastic paraplegia with dystonia linked to chromosome 2q24-2q31

Movement Disorders

Volumn 24, Issue 3, 2009, Pages 364-370

  Gilbert, Donald L ^a   Leslie, Elizabeth J ^a   Keddache, Mehdi ^a   Leslie, Nancy D ^a  

^a UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

Author keywords

Deep brain stimulation; Dystonia; Genetics; Linkage; Spastic paraplegias

Indexed keywords

CHIMERIN; DISTAL LESS HOMEOBOX 1 TRANSCRIPTION FACTOR; GUANINE NUCLEOTIDE EXCHANGE FACTOR; RAP GUANINE NUCLEOTIDE EXCHANGE FACTOR; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG; PRIMER DNA;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BRAIN DEPTH STIMULATION; CHILD; CHROMOSOMAL LOCALIZATION; CHROMOSOME 2Q; CHROMOSOME MAP; CLINICAL ASSESSMENT; DISEASE DURATION; DYSTONIA; FEMALE; GENE LOCUS; GENE SEGREGATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; LINKAGE ANALYSIS; MALE; MICROSATELLITE MARKER; MUSCLE WEAKNESS; NEUROPATHOLOGY; ONSET AGE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SPASTICITY; TREATMENT RESPONSE; CHROMOSOME 2; GENETIC LINKAGE; GENETICS; GENOTYPE; HAPLOTYPE; MIDDLE AGED; NEUROLOGIC EXAMINATION; PEDIGREE; PHENOTYPE; TRINUCLEOTIDE REPEAT; VIDEORECORDING;

ADOLESCENT; ADULT; CHILD; CHROMOSOMES, HUMAN, PAIR 2; DNA PRIMERS; DYSTONIA; FEMALE; GENOTYPE; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); MALE; MIDDLE AGED; NEUROLOGIC EXAMINATION; PEDIGREE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; SPASTIC PARAPLEGIA, HEREDITARY; TRINUCLEOTIDE REPEAT EXPANSION; VIDEOTAPE RECORDING; YOUNG ADULT;

EID: 67651099235     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.22363     Document Type: Article

References (13)

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