Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen
- 1 April 2008
- journal article
- Published by Elsevier BV in The Lancet Neurology
- Vol. 7 (4), 319-326
- https://doi.org/10.1016/s1474-4422(08)70048-6
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosisNature Genetics, 2007
- ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association studyThe Lancet Neurology, 2007
- Whole-Genome Analysis of Sporadic Amyotrophic Lateral SclerosisNew England Journal of Medicine, 2007
- Amyotrophic lateral sclerosis as a complex genetic diseaseBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 2006
- Molecular biology of amyotrophic lateral sclerosis: insights from geneticsNature Reviews Neuroscience, 2006
- ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosisNature Genetics, 2006
- Molecular and cellular pathways of neurodegeneration in motor neurone diseaseJournal of Neurology, Neurosurgery & Psychiatry, 2005
- VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic deathNature Genetics, 2003
- British motor neuron disease twin study.Journal of Neurology, Neurosurgery & Psychiatry, 1997
- Dose-ranging study of riluzole in amyotrophic lateral sclerosisThe Lancet, 1996