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Self-reported functioning among patients with ultra-rare nemaline myopathy or a related disorder in Finland: a pilot study
BACKGROUND: Nemaline myopathy (NM) and related disorders (NMr) form a heterogenous group of ultra-rare (1:50,000 live births or less) congenital muscle disorders. To elucidate the self-reported physical, psychological, and social functioning in the daily lives of adult persons with congenital muscle...
Autores principales: | Lehtokari, Vilma-Lotta, Similä, Minna, Tammepuu, Marianne, Wallgren-Pettersson, Carina, Strang-Karlsson, Sonja, Hiekkala, Sinikka |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10691147/ https://www.ncbi.nlm.nih.gov/pubmed/38037113 http://dx.doi.org/10.1186/s13023-023-02973-2 |
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