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Figure 4 | BMC Neurology

Figure 4

From: Transient, recurrent, white matter lesions in x-linked Charcot-Marie-tooth disease with novel mutation of gap junction protein beta 1 gene in China: a case report

Figure 4

Chromatograms of a Cx32 mutation. The arrow in chromatogram A represents the mutation site (T to G transition at nucleotide 278) in the male Chinese patient with X-linked Charcot-Marie-Tooth disease. The arrow in chromatogram B represents the site of a T278G heterozygous mutation in the patient’s mother.

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BMC Neurology

ISSN: 1471-2377

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