Genetic linkage

Citations 1-10 of 69 total displayed.

Most recent content (6 Jan 2009):

EDITORIALS
A new disease mimicking Refsum syndrome

Thomas D. Bird
Neurology 2009; 72: 13. [Full text] [PDF]  

ARTICLES
A novel Refsum-like disorder that maps to chromosome 20

T. Fiskerstrand, P. Knappskog, J. Majewski, R. J. Wanders, H. Boman, and L. A. Bindoff
Neurology 2009; 72: 20-27. [Abstract] [Full text] [PDF]  

Past content (since Jan 2001):

ARTICLES
Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1

D. S. Stamm, C. M. Powell, J. M. Stajich, V. L. Zismann, D. A. Stephan, B. Chesnut, A. S. Aylsworth, S. G. Kahler, K. L. Deak, J. R. Gilbert, and M. C. Speer
Neurology 2008; 71: 1764-1769. [Abstract] [Full text] [PDF]  

ARTICLES
Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2

H. Houlden, M. Laura, F. Wavrant–De Vrièze, J. Blake, N. Wood, and M. M. Reilly
Neurology 2008; 71: 1660-1668. [Abstract] [Full text] [PDF]  

ARTICLES
A novel dominant mutation of the Na_v1.4 -subunit domain I leading to sodium channel myotonia

S. Petitprez, L. Tiab, L. Chen, L. Kappeler, K. M. Rösler, D. Schorderet, H. Abriel, and J-M Burgunder
Neurology 2008; 71: 1669-1675. [Abstract] [Full text] [PDF]  

VIEWS & REVIEWS
Update on blepharospasm: Report from the BEBRF International Workshop

Mark Hallett, Craig Evinger, Joseph Jankovic, and Mark Stacy
Neurology 2008; 71: 1275-1282. [Abstract] [Full text] [PDF]  

EDITORIALS
Genetic testing for the spastic paraplegias: Drowning by numbers

Alexandra Dürr
Neurology 2008; 71: 236-238. [Full text] [PDF]  

ARTICLES
A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23

K. J. Dick, R. Al-Mjeni, W. Baskir, R. Koul, M. A. Simpson, M. A. Patton, S. Raeburn, and A. H. Crosby
Neurology 2008; 71: 248-252. [Abstract] [Full text] [PDF]  

EDITORIALS
Late-onset HMSN 2: Further evidence of genetic heterogeneity

Peter J. Dyck
Neurology 2008; 71: 9-10. [Full text] [PDF]  

ARTICLES
Late-onset hereditary axonal neuropathies

C. L. Bennett, V. H. Lawson, K. L. Brickell, K. Isaacs, W. Seltzer, H. P. Lipe, M. D. Weiss, G. T. Carter, K. M. Flanigan, P. F. Chance, and T. D. Bird
Neurology 2008; 71: 14-20. [Abstract] [Full text] [PDF]  

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