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LRP4 antibodies in serum and CSF from amyotrophic lateral sclerosis patients
OBJECTIVE: Amyotrophic lateral sclerosis (ALS) and myasthenia gravis (MG) are caused, respectively, by motor neuron degeneration and neuromuscular junction (NMJ) dysfunction. The membrane protein LRP4 is crucial in the development and function of motor neurons and NMJs and LRP4 autoantibodies have b...
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| Hlavní autoři: | , , , , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BlackWell Publishing Ltd
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4212481/ https://ncbi.nlm.nih.gov/pubmed/25356387 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.26 |
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