New point mutations and deletions of the connexin 32 gene in x-linked charcot-marie-tooth neuropathy
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference12 articles.
1. X-linked dominant Charcot Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq;Gal;Hum Genet,1985
2. X-linked neuropathy: gene localization with DNA probes;Fischbeck;Ann Neurol,1986
3. Mapping of the gene for X-linked dominant Charcot-Marie-Tooth neuropathy;Ionasescu;Neurology,1992
4. Localization of X-linked Charcot-Marie-Tooth Disease to Xq13.1 [abstract];Bergoffen;Am J Hum Genet,1993
5. A neurological gene map;Rosenberg;Arch Neurol,1993
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