Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes
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R. Płoski | P. Tonin | M. Neri | M. Rydzanicz | T. Stokłosa | J. Kosińska | M. Romanelli | F. Gualandi | V. Guglielmi | L. Verriello | A. Sangalli | E. Pancheri | G. Tomelleri | G. Vattemi | M. Machnicki | K. Pruszczyk