Identification of myosin heavy chain post-translational modifications in patients with MHY mutations
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https://www.omicsdi.org/dataset/pride/PXD039178
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资源简介：
Congenital myopathies are rare genetic muscle diseases notably due to mutations in the MYH2 gene. Here we assessed their myosin heavy chain post-translational modifications. For that, we purified beta/slow and type IIa myosin heavy chains from limb muscles of five patients and five healthy controls. We then ran a LC/MS analysis.
创建时间：
2023-01-30
