Patients’ lived experience of thymidine kinase 2 deficiency: the online survey-based assessment of TK2d patient perspectives study
Background: Thymidine kinase 2 deficiency (TK2d) is an ultra-rare autosomal recessive mitochondrial disease characterized by progressive myopathy. Objectives: To understand patient experiences and the impact of TK2d on patient quality of life (QoL), and to explore support needs. Design: A cross-sect...
সংরক্ষণ করুন:
| প্রধান লেখক: | , , , , , , |
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| বিন্যাস: | Artigo |
| ভাষা: | Inglês |
| প্রকাশিত: |
SAGE Publishing
2026-07-01
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| মালা: | Therapeutic Advances in Rare Disease |
| অনলাইন ব্যবহার করুন: | https://doi.org/10.1177/26330040261469197 |
| ট্যাগগুলো: |
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