Ultrastructural PMP22 expression in inherited demyelinating neuropathies

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1A TECHNIQUE FOR ULTRACRYOTOMY OF CELL SUSPENSIONS AND TISSUES1973 · 1,094 citations
2. 2Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 171994 · 312 citations
3. 3Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP)2008 · 51 citations
4. 4Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group.1992 · 41 citations
5. 5Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion1995 · 113 citations