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Diagnostic approach for FSHD revisited: SMCHD1 mutations cause FSHD2 and act as modifiers of disease severity in FSHD1
Mirjam Larsen*, Simone Rost, Nady El Hajj, Andreas Ferbert, Marcus Deschauer, Maggie C. Walter, Benedikt Schoser, Pawel Tacik, Wolfram Kress, Clemens R. Müller
*Corresponding author for this work
Research output: Contribution to journal › Article › peer-review
80
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(Scopus)