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Novel truncating mutations of MYO18B causing congenital myopathy in a Swiss patient

Detalles Bibliográficos
Autores principales:	Mihaylova, Violeta, Chablais, Fabian, Herenger, Yvan, Spiegel, Roland, Heinrich Jung, Hans
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer 2020
Materias:	Clinical/Scientific Notes
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7323478/ https://www.ncbi.nlm.nih.gov/pubmed/32637634 http://dx.doi.org/10.1212/NXG.0000000000000458

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