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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Autors principals: 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
Idioma:Inglês
Publicat: 2011
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Article
Accés en línia: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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