Human homologue of a gene mutated in the slow Wallerian degeneration (C57BL/Wlds) mouse

Febilla Fernando(Utrecht University), Michael P. Coleman(Babraham Institute), Laura Conforti(University of Cincinnati), Sabrina Tosi(MRC Human Immunology Unit), A. David Smith(Emory University)

Gene

February 1, 2002

10.1016/s0378-1119(02)00394-3

Cited by 25

Related Papers

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

|Nature Genetics|2009|3.4k

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

|Nature Genetics|2011|2.1k

Facts and Recommendations about Total Homocysteine Determinations: An Expert Opinion

|Clinical Chemistry|2004|1.1k

dSarm/Sarm1 Is Required for Activation of an Injury-Induced Axon Death Pathway

|Science|2012|722

Wallerian degeneration: an emerging axon death pathway linking injury and disease

|Nature reviews. Neuroscience|2014|627