A novel late-onset axial myopathy associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene
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B. Engelen | F. Muntoni | N. Voermans | G. Dekomien | E. Kamsteeg | H. Jungbluth | C. Sewry | S. Lillis | V. Straub | C. Jonsrud | P. Maddison | M. Lammens | M. Visser | S. Lindal | S. Løseth | T. Torbergsen | A. Radunović | M. Broman