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Evidence of a founder haplotype refines the X-linked Charcot–Marie-Tooth (CMTX3) locus to a 2.5 Mb region
X-linked Charcot–Marie-Tooth (CMTX) disease is a common inherited degenerative disorder of the peripheral nerve. Previously, our laboratory identified a large New Zealand/United Kingdom (NZ/UK) family mapping to the CMTX3 locus (Xq26.3–27.1). We have now identified a second large, Australian X-linke...
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| Vydáno v: | Neurogenetics |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2008
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6852654/ https://ncbi.nlm.nih.gov/pubmed/18458969 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10048-008-0126-4 |
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