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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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Bibliografski detalji
Izdano u:Neurogenetics
Glavni autori: Brewer, Megan, Changi, Febriani, Antonellis, Anthony, Fischbeck, Kurt, Polly, Patsie, Nicholson, Garth, Kennerson, Marina
Format: Artigo
Jezik:Inglês
Izdano: 2008
Teme:
Online pristup: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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