Neuropathy in Human and Mice with PMP22 null

BACKGROUND/OBJECTIVE: Haploinsufficiency of PMP22 causes hereditary neuropathy with liability to pressure palsies (HNPP). However, the biological functions of PMP22 in humans are largely unexplored due to the absence of patients with PMP22 null mutations. DESIGN, SETTING AND PARTICIPANTS: We have ev...

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Detaylı Bibliyografya
Asıl Yazarlar: Saporta, Mario Andre, Katona, Istvan, Zhang, Xuebao, Roper, Helen P., Carr, Louise, Macdonald, Fiona, Brueton, Louise, Blake, Julian, Suter, Ueli, Reilly, Mary M., Shy, Michael E., Li, Jun
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2011
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3711535/
https://ncbi.nlm.nih.gov/pubmed/21670407
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archneurol.2011.110
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