ISSN:
1546-1718
Source:
Nature Archives 1869 - 2009
Topics:
Biology
,
Medicine
Notes:
[Auszug] Sir — Charcot-Marie-Tooth disease type 1 (CMT1)1 is a genetically heterogeneous peripheral neuropathy involving mutations in the genes encoding peripheral myelin protein 22 (PMP22), myelin protein zero (MPZ) and connexin 32 (Cx32) on chromosomes 17pll.2, lq22–23 and Xql3.1, ...
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1038/ng0197-13