Proof of genetic heterogeneity in X-linked Charcot–Marie–Tooth disease

Inken G. Huttner, Marina Kennerson, Stephen Reddel, D. Radovanovic, Garth A. Nicholson

Neurology · 2006 · 32 citations · 24 references

Abstract

This study is the first to confirm the CMTX3 locus and to refine the genetic interval to a 5.7-Mb region flanked by the markers DXS1041 and DXS8106. GJB1 mutation-negative forms of X-linked CMT, such as CMTX3, may account for a significant proportion of X-linked CMT.

References

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