Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia loci

American Journal of Medical Genetics

Volumn 102, Issue 1, 2001, Pages 68-72

  Patel, H ^a   Hart, P E ^b   Warner, T ^c   Allen, I ^d   Phillimore, H E ^a   Silver, J R ^b   Wood, N W ^c   Jeffery, S ^d   Patton, M A ^a   Crosby, A H ^b,e  

^a ST GEORGE S HOSPITAL   (United Kingdom)

^b ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

^c Chiltern Hospital   (United Kingdom)

^d UNIVERSITY COLLEGE LONDON   (United Kingdom)

^e ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

Hereditary spastic paraplegia; Linkage mapping; Silver syndrome

Indexed keywords

ADULT; AGED; ARTICLE; CHROMOSOME; CLINICAL ARTICLE; FEMALE; GENE; GENETIC LINKAGE; GENOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; SILVER RUSSELL SYNDROME;

ADULT; AGED; AGED, 80 AND OVER; FAMILY HEALTH; FEMALE; GENES, DOMINANT; GENOME, HUMAN; HAND; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MICROSATELLITE REPEATS; MIDDLE AGED; MUSCULAR DISEASES; PEDIGREE; PHENOTYPE; SPASTIC PARAPLEGIA, HEREDITARY; SYNDROME;

EID: 0035934020     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20010722)102:1<68::AID-AJMG1411>3.0.CO;2-R     Document Type: Article

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3. A procedure for combining two-point lod scores into a summary multipoint map
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5. A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34
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10. Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p
11. Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity
12. X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene
13. Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-q15
14. Hereditary ataxias and paraplegias in Cantabria, Spain. An epidemiological and clinical study
15. A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13 and evidence of further genetic heterogeneity
16. A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13
17. X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic at the proteolipid protein locus
18. The role of mitochondrial dysfunction and neuronal nitric oxide in animal models of neurodegenerative diseases
19. Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy
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21. A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28