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A rare structural myopathy: Nemaline myopathy
Nemaline myopathy, which is characterized by the accumulation of ‘’rod’’ bodies in muscle fibers is a very rare inherited muscle disease. According to the underlying mutation, the disease has varying severity of clinical outcomes. Patients with severe forms of the disease die because of hypotonia, f...
Tallennettuna:
| Julkaisussa: | Turk Pediatri Ars |
|---|---|
| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Kare Publishing
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6559969/ https://ncbi.nlm.nih.gov/pubmed/31217710 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/TurkPediatriArs.2018.4402 |
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