Hereditary spastic paraplegia: The pace quickens

Annals of Neurology

Volumn 51, Issue 6, 2002, Pages 669-672

  Fink, John K ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EDITORIAL; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MUSCLE SPASM; MUSCLE WEAKNESS; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; SYNDROME; SYNDROME DELINEATION;

ADENOSINE TRIPHOSPHATASES; ANIMALS; CALCIUM-BINDING PROTEINS; CHILD; GENES, DOMINANT; GENES, RECESSIVE; GTP PHOSPHOHYDROLASES; HUMANS; METALLOENDOPEPTIDASES; MUTATION; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 0036267195     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.10258     Document Type: Editorial

References (14)

1. Sklerose der seitenstrange des ruckenmarks bei vier kindern derselben familie
2. Hereditary spastic paraplegia
3. Classification of the hereditary ataxias and paraplegias
4. A novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q22-q34
5. Hereditary spastic paraplegia: Genetic heterogeneity and genotype-phenotype correlation
6. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
7. Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics
8. Spastin, a new AAA protein, binds to α and β tubulins
9. Mutations in a novel GTPase cause autosomal dominant hereditary spastic paraplegia
10. Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia
11. Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease
12. A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3
13. Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60
14. Linkage of AD HSP and cognitive impairment to chromosome 2p: Haplotype and phenotype analysis indicates variable expression and low or delayed penetrance