Loss‐of‐function variants in SPTAN1 and SPTBN4 cause early‐onset hereditary myopathy

Fuente: Wiley Open Access

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Bibliographic Details
Main Authors:	Jonathan De Winter, Johanna Palmio, Markus Schuelke, Bjarne Udd, Werner Stenzel, Jonathan Baets
Format:	Artículo Open Access
Published:	Wiley 2025
Subjects:	The Journal of Physiology
Online Access:	Acceder al recurso
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