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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Bibliografski detalji
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: 2011
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Article
Online pristup: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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