C A Garcia

Periaxin mutations cause recessive Dejerine-Sottas neuropathy.

S M Leber, P. Stankiewicz, J. Lupski, 2001, American journal of human genetics.

Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 gene.

J. Lupski, E. Shooter, P. Patel, 1993, The New England journal of medicine.

Charcot-Marie-Tooth disease and related inherited neuropathies.

J. Lupski, L. Reiter, C A Garcia, 1996, Medicine.