A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations-Reference-Cited by-同舟云学术

A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations

Published:2009-12-04 Issue:4 Volume:17 Page:541-549
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:

Author:

Brussino A.,Vaula G.,Cagnoli C.,Panza E.,Seri M.,Di Gregorio E.,Scappaticci S.,Camanini S.,Daniele D.,Bradac G. B.,Pinessi L.,Cavalieri S.,Grosso E.,Migone N.,Brusco A.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2009.02844.x/fullpdf

Reference20 articles.

1. Leukodystrophies: clinical and genetic aspects;Lyon;Top Magn Reson Imaging,2006

2. Lamin B1 duplications cause autosomal dominant leukodystrophy;Padiath;Nat Genet,2006

3. A novel duplication confirms the involvement of 5q23.2 in autosomal dominant leukodystrophy;Meijer;Arch Neurol,2008

4. A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathy;Brussino;J Neurol Neurosurg Psychiatry,2009

5. Dominantly inherited leukodystrophy showing cerebellar deficits and spastic paraparesis: a new entity?;Fukazawa;J Neurol,1997

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