Garth Nicholson

发表

Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6

Xun Hu, Kelly L. Williams, Christopher E. Shaw, 2009, Science.

Christine Klein, Karen Ostergaard, Stuart, 2006 .

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease

Danqing Zhu, Stephan Züchner, M. Pericak-Vance, 2005, Nature Genetics.

TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis

Xun Hu, Kelly L. Williams, Christopher E. Shaw, 2008, Science.

Replication of association between ELAVL4 and Parkinson disease: the GenePD study

Christine Klein, David J. Burn, Kenneth B. Baker, 2008, Human Genetics.

Mutation screening of the N‐myc downstream‐regulated gene 1 (NDRG1) in patients with Charcot‐Marie‐Tooth Disease

Hanns Lochmüller, Thomas Voit, P K Thomas, 2003, Human mutation.