SCOPUS 정보 검색 플랫폼

Neurology

Volumn 67, Issue 11, 2006, Pages 1912-1913

The spastin jigsaw puzzle: Another missing piece found

(1) Hedera, Peter a,b

a VANDERBILT UNIVERSITY MEDICAL CENTER (United States)

b VANDERBILT UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL ADHESION MOLECULE; PROTEOLIPID PROTEIN; SPASTIN;

AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 2P; EDITORIAL; GENE; GENE DELETION; GENE DOSAGE; GENE INSERTION; GENE MUTATION; GENETIC RECOMBINATION; GENOTYPE PHENOTYPE CORRELATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; LIGATION; MICROTUBULE; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; PROTEIN BINDING; SPAST GENE;

ADENOSINE TRIPHOSPHATASES; HUMANS; MUTATION; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 33845692940 PISSN: 00283878 EISSN: None Source Type: Journal
DOI: 10.1212/01.wnl.0000251270.66773.cc Document Type: Editorial

Times cited : (1)

References (10)

1
- 0032721512
- Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
- Hazan J, Fonknechten N, Mavel D, et al. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. Nat Genet 1999;23:296-303.
- (1999) Nat Genet , vol.23 , pp. 296-303
- Hazan, J.¹ Fonknechten, N.² Mavel, D.³

2
- 8944250670
- Hereditary spastic paraplegia: Advances in genetic research
- Fink JK, Heiman-Patterson T, Bird T, et al. Hereditary spastic paraplegia: advances in genetic research. Neurology 1996;46:1507-1514.
- (1996) Neurology , vol.46 , pp. 1507-1514
- Fink, J.K.¹ Heiman-Patterson, T.² Bird, T.³

3
- 0032708407
- Hereditary spastic paraplegia: Heterogeneity and genotype/phenotype correlation
- Fink JK, Hedera P. Hereditary spastic paraplegia: heterogeneity and genotype/phenotype correlation. Semin Neurol 1999;19:301-310.
- (1999) Semin Neurol , vol.19 , pp. 301-310
- Fink, J.K.¹ Hedera, P.²

4
- 2942531080
- Hereditary spastic paraplegia: Spastin phenotype and function
- Fink JK, Rainier S. Hereditary spastic paraplegia: spastin phenotype and function. Arch Neurol 2004;61:830-833.
- (2004) Arch Neurol , vol.61 , pp. 830-833
- Fink, J.K.¹ Rainier, S.²

5
- 25844529535
- Microtubules cut and run
- Baas PW, Karabay A, Qiang L. Microtubules cut and run. Trends Cell Biol 2005;15:518-524.
- (2005) Trends Cell Biol , vol.15 , pp. 518-524
- Baas, P.W.¹ Karabay, A.² Qiang, L.³

6
- 0034163576
- Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia
- Fonknechten N, Mavel D, Byrne P, et al. Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia. Hum Mol Genet 2000;1:637-644.
- (2000) Hum Mol Genet , vol.1 , pp. 637-644
- Fonknechten, N.¹ Mavel, D.² Byrne, P.³

7
- 33845696394
- High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia
- Beetz C, Nygren AOH, Schickel J, et al. High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia. Neurology 2006;67:1926-1930.
- (2006) Neurology , vol.67 , pp. 1926-1930
- Beetz, C.¹ Nygren, A.O.H.² Schickel, J.³

8
- 2342578875
- MLPA and MAPH: New techniques for detection of gene deletions
- Sellner LN, Taylor GR. MLPA and MAPH: new techniques for detection of gene deletions. Hum Mutat 2004;23:413-419.
- (2004) Hum Mutat , vol.23 , pp. 413-419
- Sellner, L.N.¹ Taylor, G.R.²

9
- 0035184654
- Mutation in a novel GTPase cause autosomal dominant hereditary spastic paraplegia
- Zhao X, Alvarado D, Rainier S, et al. Mutation in a novel GTPase cause autosomal dominant hereditary spastic paraplegia. Nat Genet 2001;29:326-331.
- (2001) Nat Genet , vol.29 , pp. 326-331
- Zhao, X.¹ Alvarado, D.² Rainier, S.³

10
- 0032796376
- Alu repeats and human disease
- Deininger PL, Batzer MA. Alu repeats and human disease. Mol Genet Metab 1999;67:183-193.
- (1999) Mol Genet Metab , vol.67 , pp. 183-193
- Deininger, P.L.¹ Batzer, M.A.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.