A new mutation of the SCGA gene is the cause of a late onset mild phenotype limb girdle muscular dystrophy type 2D with axial involvement

Lidia Gonzalez-Quereda, Eduard Gallardo, Ana Töpf, Alicia Alonso-Jimenez, Volker Straub, Maria Jose Rodriguez, Cinta Lleixa, Isabel Illa, Pia Gallano, Jordi Diaz-Manera

Research output: Contribution to journal › Article › Research › peer-review

7 Citations (Scopus)

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Medicine & Life Sciences