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A novel locus for X-linked recessive CMT with deafness and optic neuropathy maps to Xq21.32-q24
Neurology Kim et al. 64: 1964
Data Supplement
Two figures and one table; two Word documents and one TIF image.
Files in this Data Supplement:
E1
- Figure 1; Word document.
E2
- Figure 2; TIF file.
E3
- E-Table 1: Two-point lod scores between the X-linked recessive CMT in this family and the short tandem repeat markers on the chromosome region Xq21.1-q26.3; Word document.
This Article
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