A point mutation in the human connexin32 promoter P2 does not correlate with X-linked dominant Charcot-Marie-Tooth neuropathy in Germany.

Source:http://linkedlifedata.com/resource/pubmed/id/11295246

Brain Res. Mol. Brain Res. 2001 Mar 31 88 1-2 183-5

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PMID
11295246