Llwytho...
Homozygous Recessive MYH2 Mutation Mimicking Dominant MYH2 Associated Myopathy
Mutations in MYH2 that encodes myosin heavy chain IIa cause both dominant and recessively inherited myopathies. Patients with dominantly inherited MYH2 missense mutations present with ophthalmoplegia and progressive proximal limb weakness. Muscle biopsy reveals rimmed vacuoles and inclusions, prompt...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Neuromuscul Disord |
|---|---|
| Prif Awduron: | , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2018
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6466613/ https://ncbi.nlm.nih.gov/pubmed/29934118 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nmd.2018.05.006 |
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