Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle α-actin (ACTA1) gene
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Susan C. Brown | K. Pelin | E. Mercuri | F. Muntoni | N. Laing | C. Wallgren‐Pettersson | V. Dubowitz | A. Manzur | H. Jungbluth | C. Sewry | S. Brown | K. Nowak | Eugenio Mercuri | E. Mercuri