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Neuromuscular Junction Changes in a Mouse Model of Charcot-Marie-Tooth Disease Type 4C
The neuromuscular junction (NMJ) appears to be a site of pathology in a number of peripheral nerve diseases. Charcot-Marie-Tooth (CMT) 4C is an autosomal recessive, early onset, demyelinating neuropathy. Numerous mutations in the SH3TC2 gene have been shown to underlie the condition often associated...
Tallennettuna:
| Julkaisussa: | Int J Mol Sci |
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| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
MDPI
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6320960/ https://ncbi.nlm.nih.gov/pubmed/30562927 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms19124072 |
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